Compositions and assays to detect swine h1n1 influenza a virus, seasonal h1 influenza a virus and seasonal h3 influenza a virus nucleic acids

ABSTRACT

Methods for detecting the presence or absence of the swine H1N1 influenza A virus, seasonal H1 influenza A virus and/or seasonal H3 influenza A virus nucleic acids in biological samples are disclosed. Compositions that are target-specific nucleic acid sequences and kits comprising target-specific nucleic acid oligomers for amplifying in vitro the swine H1N1 influenza A virus, seasonal H1 influenza A virus and/or seasonal H3 influenza A virus nucleic acid and detecting amplified nucleic acid sequences are disclosed.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit under 35 U.S.C. §119(e) ofprovisional application No. 61/363,628, filed Jul. 12, 2010, thecontents of which are incorporated herein by reference.

FIELD

The present invention is directed to the field of detecting infectiousagents, more specifically by using compositions and methods to detectviruses including the swine H1N1 influenza A virus, seasonal H1influenza A virus and/or seasonal H3 influenza A virus.

BACKGROUND

Influenza viruses (types A, B, and C) are members of theorthomyxoviridae family that cause influenza. Type A influenza virusesinfect birds and mammals, including humans, whereas types B and C infecthumans only. Influenza viruses are roughly spherical enveloped virusesof about 8-200 nm diameter that contain segmented negative sense genomicRNA. The envelope contains rigid structures that include hemagglutinin(HA) and neuraminidase (NA). Combinations of HA and NA subtypes, whichresult from genetic reassortment, are used to characterize viralisolates. Generally, influenza viral isolates are identified bynomenclature that includes type, location, isolate number, isolationyear, and HA and NA subtypes (e.g., “A/Sydney/7/97(H3N2)” refers to typeA, from Sydney, isolate 7, in 1997, with HA 3 and NA 2 subtypes). Thecommon nomenclature for HA and NA uses the first letter of the genefollowed by the subtype number (e.g., H#, N# where # is a number). Minorgenetic changes that produce antigenic drift may cause influenzaepidemics, whereas genetic changes that result in a new HA or NA subtypeproduce antigenic shift that may cause a pandemic. Analysis of humaninfluenza virus A infections has shown that a few HA and NA combinationsare clinically significant in causing pandemics during the 1900s, i.e.,H1N1 in 1918, H2N2 in 1957, and H3N2 in 1968.

Influenza viruses that infect birds (e.g., chickens, ducks, pigeons) usecombinations of H5, H7 or H9 with any of N1 to N9. Since 1997, avianinfluenza viruses that have infected humans have included H5N1, H9N2,H7N2, and H7N7 viruses. Even limited human infections caused by an avianinfluenza virus raise concern for a potential pandemic, resulting inquarantines, and intentional destruction of large numbers of fowl, withaccompanying hardship. An avian influenza virus, or variant derivedtherefrom, that efficiently transfers by human-to-human contact couldcause a pandemic (Li et al., 2003, J. Virol. 77(12): 6988-6994).

The structure of an influenza virion is generally well understood. InInfluenza A, there are generally eight genes, called RNA segments: theHA gene, the NA gene, the NP gene, the M gene, the NS gene, and thegenes for the subunits of RNA polymerase, PA, PB1, PB1-F2 and PB2. TheHA gene encodes the protein hemagglutinin, which is generally present asa glycoprotein. The NA gene encodes neuraminidase (NA), anotherglycoprotein. Both are found on the virion surface. The NP gene encodesthe nucleoprotein. The nucleoproteins of Influenza A, B, and C aredifferent. The M gene encodes for both the M1 protein and the M2protein, depending on the reading frame. The M1 protein is the matrixprotein, which provides a structure underlying the lipid bilayer. The M2protein is an ion channel embedded in the lipid bilayer. The NS geneencodes multiple proteins (depending on the reading frame) which arefound in the cytosol of an infected cell but not within the virionitself. Each RNA segment consists of RNA joined with several proteins,such as the proteins for RNA polymerase (PB1, PB2, and PA) and NP. Dueto the high mutation rate of virus strains, within a given time periodand within a given RNA segment, there may be areas of high variationbetween the sequences found in different sample organisms, and there maybe areas which are consistent among the sequences found in differentsample organisms.

Due to this variation, Influenza epidemics occur yearly; although bothtypes A and B circulate in the population, type A is usually dominant.These yearly epidemics are partly due to antigenic variation in the HAand NA surface proteins of the virus. In March of 2009, a novelInfluenza A virus (2009 H1N1 influenza virus) emerged in North Americaand globally. (Centers for Disease Control and Prevention. 2009. SwineInfluenza A (H1N1) Infection in Two Children—Southern California,March-April 2009. MMWR 58 (Dispatch); 1-3.) The 2009 H1N1 influenzavirus is considered a reassortment virus composed of two genes frominfluenza viruses that normally circulate in swine in Europe and Asia inaddition to bird (avian) and human genes. The 2009 H1N1 influenza virusis also considered an Influenza Virus of Swine Origin (SOIV). Thesymptoms for the 2009 H1N1 virus are similar to those of seasonalinfluenza strains, however diarrhea and vomiting may be more commonlyreported with the 2009 H1N1 virus.

Human influenza viruses produce highly contagious, acute respiratorydisease that results in significant morbidity and economic costs, withsignificant mortality among very young, elderly, and immuno-compromisedsubpopulations. A typical influenza virus infection in humans has ashort incubation period (1 to 2 days) and symptoms that last about aweek (e.g., abrupt onset of fever, sore throat, cough, headache,myalgia, malaise and anorexia), which may lead to pneumonia causingincreased morbidity and mortality in pediatric, elderly, andimmuno-compromised populations. With the 2009 H1N1 virus, youngchildren, pregnant women, and those with underlying health conditionsmay be at greater risk for severe complications. Optimal protectionagainst infection requires annual inoculation with a vaccine thatincludes a combination of types A and B of the most likely subtypes forthat year, based on global epidemiological surveillance. To be effectivein treatment, pharmaceuticals that block viral entry into cells ordecrease viral release from infected cells must be administered within48 hrs of symptoms onset. Such antiviral agents may include oseltamivir(trade name TAMIFLU™, zanamivir (RELENZA™, amantadine and rimantadine,which have been approved for use in the United States for treatinginfluenza. The CDC recommends the use of oseltamivir or zanamivir forpatients with the 2009 H1N1 influenza virus as this virus is resistantto amantadine and rimantadine. It is apparent, then, that properidentification of the influenza strain causing an infection is useful indetermining the proper course of treatment.

A variety of methods have been used to detect influenza virusesclinically. Viral culture in vitro (in monkey kidney cells) followed byvisual analysis and/or hemadsorption using microbiological methods candetect influenza viruses A and B in specimens (e.g., nasopharyngeal orthroat swab, nasal or bronchial wash, nasal aspirate, or sputum). Otherdetection tests include immunofluorescence assays (IFA), enzymeimmunoassays (EIA), and enzyme-linked immunosorbent assays (ELISA) thatuse antibodies specific to influenza virus antigens. Examples include asandwich microsphere-based IFA that uses influenza A- or B-specificmonoclonal antibodies and flow cytometry (Yan et al., 2004, J. Immunol.Methods 284(1-2): 27-38), monoclonal antibody-based EIA tests(DIRECTIGEN® FLU A and DIRECTIGEN® FLU A+B, Becton, Dickinson and Co.,Franklin Lakes, N.J., and QUICKVUE® Influenza Test, Quidel, San Diego,Calif.), and an immunoassay that produces a color change due toincreased thickness of molecular thin films when an immobilized antibodybinds an influenza A or B nucleoprotein (FLU OIA®, Biostar Inc.,Boulder, Colo.). Another chromagenic assay detects viral NA activity bysubstrate cleavage (ZSTAT FLU®, ZymeTx, Inc., Oklahoma City, Okla.).Assays are known that rely on reverse-transcriptase polymerase chainreactions (RT-PCR) to amplify influenza viral sequences to detectinfluenza A and B viruses (e.g., Templeton et al., 2004, J. Clin.Microbiol. 42(4):1564-69; Frisbie et al., 2004, J. Clin. Microbiol.42(3):1181-84; Boivin et al., 2004, J. Clin. Microbiol., 42(1):45-51;Habib-Bein et al., 2003, J. Clin. Microbiol. 41(8):3597-3601; Li et al.,2001, J. Clin. Microbiol. 39(2):696-704; van Elden et al., 2001, J.Clin. Microbiol. 39(1): 196-200; Fouchier et al., 2000, J. Clin.Microbiol. 38(11):4096-101; Ellis et al., 1997, J. Clin. Microbiol.35(8): 2076-2082; PCT Nos. WO 2004 057021, WO 02 00884, WO 00 17391, andWO 97/16570, EP Publ. No. 1 327 691 A2, U.S. Pat. No. 6,015,664, andPROFLU-1™ and HEXAPLEX™ tests, Prodesse, Milwaukee, Wis.). Serologydetects seroconversion associated with 2009 H1N1 influenza virus,seasonal H1 influenza A and/or seasonal H3 influenza A virus infectionsby detecting antibodies present in acute and convalescent sera frompatients with influenza symptoms. Detection methods have associatedadvantages and disadvantages related to sensitivity, specificity, assayand handling time, required equipment, and exposure of technicalpersonnel to infectious agents with related safety requirements forlaboratories and personnel. Generally, culture and serological testsrequire longer completion times (5 days to 2 weeks) with potentiallygreater exposure of technical personnel to infectious agents.Immunoassays are generally faster (30 min to 4 hrs) but often requiresubstantial sample handling and rely on subjective determination ofresults by technical personnel. There is a need for a test that providessensitive, specific detection influenza viruses, including the 2009 H1N1influenza virus strain, in a relatively short time, with a minimum ofexposure of technical personnel to infectious agents, so that diagnosisis completed in sufficient time to permit effective therapeutictreatment of an infected person.

SUMMARY

An embodiment disclosed herein is a composition that includes at leastone nucleic acid oligomer specific for swine H1N1 influenza A virus madeup of sequences consisting of fragments of the nucleic acid sequenceencoding the NP protein or the H1 protein, specific for swine H1N1influenza A virus or their completely complementary sequences, or DNAequivalents thereof. Particular embodiments include a composition thatincludes at least one nucleic acid oligomer which targets the swine H1N1influenza A virus comprising at least 18 contiguous nucleic acids of asequence encoding the NP protein or a H1 protein which targets the swineH1N1 influenza A virus, or their completely complementary sequences, orDNA equivalents thereof. The nucleic acid oligomer which targets theswine H1N1 influenza A virus comprising at least 18 contiguous nucleicacids of the sequence encoding a NP protein or a H1 protein whichtargets the swine H1N1 influenza A virus, or its complement, may alsohave one or more additional nucleic acids at the 5′ end and/or may havea total of no more than 50 nucleic acids.

Additional particular embodiments include nucleic acid oligomers inwhich at least one oligomer is selected from the sequences consisting of(SEQ ID NOS:1, 5, 8, 12, 17, 21, 26 and 30, or SEQ ID NOS:34, 38, 42,45, 50, 54 and 59), and/or at least one oligomer is selected from thesequences consisting of (SEQ ID NOS:2, 6, 9, 13, 18, 22, 27 and 31, orSEQ ID NOS:35, 39, 43, 46, 51, 55 and 60). Another particular embodimentalso includes at least one oligomer selected from sequences consistingof (SEQ ID NOS:3, 4, 7, 10, 11, 14, 15, 16, 19, 20, 23, 24, 25, 28, 29,32 and 33, or SEQ ID NOS:36, 37, 40, 41, 44, 47, 48, 49, 52, 53, 56, 57,58, 61 and 62). In a particular embodiment that includes an oligomerselected from sequences consisting of (SEQ ID NOS:3, 4, 7, 10, 11, 14,15, 16, 19, 20, 23, 24, 25, 28, 29, 32 and 33, SEQ ID NOS: 36, 37, 40,41, 44, 47, 48, 49, 52, 53, 56, 57, 58, 61 and 62), the oligomer alsoincludes at least one detectable label joined directly or indirectly tothe oligomer sequence. A particular label is one that is detectable in ahomogeneous assay system. In one aspect, the oligomer is labeled withtwo labels that are a fluorophore and a quencher. Particular embodimentsof these compositions are kits that include at least one of thespecified nucleic acid oligomers specific for swine H1N1 influenza Avirus. Further embodiments include methods for detectably amplifying oneor more of a seasonal H1 influenza A virus, a seasonal H3 influenza Avirus or an H1N1 influenza A virus using one or more of these oligomers.

Another embodiment disclosed herein is a composition that includes atleast one nucleic acid oligomer specific for seasonal H1 influenza Avirus made up of sequences consisting of fragments of the nucleic acidsequence encoding the H1 protein of influenza A, or their completelycomplementary sequences, or DNA equivalents thereof. The nucleic acidoligomer specific for the seasonal H1 influenza A comprising at least 18contiguous nucleic acids of the nucleic acid sequence encoding the H1protein from the seasonal H1 influenza A, or its complement, may alsohave one or more additional non-influenza sequence nucleic acids at the5′ end and/or may have a total of no more than 50 nucleic acids. Furtherembodiments include methods for detectably amplifying an influenza Avirus using one or more of these oligomers.

Additional particular embodiments include at least one oligomer selectedfrom the sequences consisting of (SEQ ID NOS:63, 68 and 72) and/or atleast one oligomer selected from the sequences consisting of (SEQ IDNOS:64, 69 and 73). Another particular embodiment also includes at leastone oligomer selected from sequences consisting of (SEQ ID NOS:65, 66,67, 70, 71, 74, 75 and 76). In a particular embodiment, the oligomerselected from sequences consisting of (SEQ ID NOS: 65, 66, 67, 70, 71,74, 75 and 76) includes at least one detectable label joined directly orindirectly to the oligomer sequence. Particular embodiments include alabel that is detectable in a homogeneous assay system. In one aspect,the oligomer is labeled with two labels that are a fluorophore and aquencher. Particular embodiments of the compositions are kits thatinclude at least one of the specified nucleic acid oligomers specificfor seasonal H1 influenza A. Further embodiments include methods fordetectably amplifying an influenza A virus using one or more of theseoligomers.

Another embodiment disclosed herein is a composition that includes atleast one nucleic acid oligomer specific for seasonal H3 influenza Amade up of sequences consisting of fragments of the nucleic acidsequence encoding the H3 protein of influenza A, or their completelycomplementary sequences, or DNA equivalents thereof. The nucleic acidoligomer specific for the seasonal H3 influenza A comprising at least 18contiguous nucleic acids of the nucleic acid sequence encoding the H1protein from the seasonal H3 influenza A, or its complement, may alsohave one or more additional non-influenza sequence nucleic acids at the5′ end and/or may have a total of no more than 50 nucleic acids. Furtherembodiments include methods for detectably amplifying an influenza Avirus using one or more of these oligomers.

A particular embodiment includes at least one oligomer comprising asequence selected from the sequences consisting of (SEQ ID NOS:77, 82,85, 88, 92, 96 and 99) and/or at least one oligomer selected from thesequences consisting of (SEQ ID NOS:78, 83, 86, 89, 93, 97 and 100).Another particular embodiment also includes at least one oligomerselected from sequences consisting of (SEQ ID NOS:79, 80, 81, 84, 87,90, 91, 94, 95, 98, 101 and 102). In a particular embodiment, theoligomer selected from sequences consisting of (SEQ ID NOS:79, 80, 81,84, 87, 90, 91, 94, 95, 98, 101 and 102) includes at least onedetectable label joined directly or indirectly to the oligomer sequence.Particular embodiments include a label that is detectable in ahomogeneous assay system. In one aspect, the oligomer is labeled withtwo labels that are a fluorophore and a quencher. Particular embodimentsof the compositions are kits that include at least one of the specifiednucleic acid oligomers specific for seasonal H3 influenza A. Furtherembodiments include methods for detectably amplifying an influenza Avirus using one or more of these oligomers.

A further embodiment is a composition or a kit including at least one ofthe specified nucleic acid oligomers specific for swine H1N1 influenza Avirus which also includes at least one of the specified nucleic acidoligomers specific for seasonal H1 influenza A virus and/or at least ofthe specified nucleic acid oligomers specific for seasonal H3 influenzaA virus. In one aspect, the kit includes a primer pair. In one aspect,the kit includes a primer pair for amplifying swine H1N1 influenza Avirus, seasonal H1 influenza A virus or seasonal H3 influenza A virus.At least one primer member of the primer pair is selected from Table 1,Table 2 or Table 3, respectively. In one aspect, the kit includes aprobe. In one aspect, the kit includes a probe with a target hybridizingsequence selected from Tables 1, 2 or 3. In one aspect, the kit is amultiplex kit and includes at least two primer pairs. In one aspect, thekit is a multiplex kit and includes at least two primer pairs foramplifying two or more of swine H1N1 influenza A virus, seasonal H1influenza A virus or seasonal H3 influenza A virus. At least one primermember of one of the at least two primer pairs is selected from Tables1, 2 and/or 3. At least one primer member of two of the at least twoprimer pairs is selected from Tables 1, 2 and/or 3. At least one primermember of each of the at least two primer pairs is selected from Tables1, 2, and/or 3. In one aspect, the kit includes at least two probes,each independently having a target hybridizing sequence selected fromTables 1, 2 and/or 3. Further embodiments include methods for detectablyamplifying an influenza A virus using one or more of these oligomers.

Another embodiment is a reaction mixture for amplifying swine H1N1influenza A virus, seasonal H1 influenza A virus and/or seasonal H3influenza A virus, wherein the reaction mixture includes at least one ofthe specified nucleic acid oligomers specific for swine H1N1 influenza Avirus which also includes at least one of the specified nucleic acidoligomers specific for seasonal H1 influenza A and/or at least of thespecified nucleic acid oligomers specific for seasonal H3 influenza A.In one aspect, the reaction mixture includes a primer pair. In oneaspect, the reaction mixture includes a primer pair for amplifying swineH1N1 influenza A virus, seasonal H1 influenza A virus or seasonal H3influenza A virus. At least one primer member of the primer pair isselected from Table 1, Table 2 or Table 3, respectively. In one aspect,the reaction mixture includes a probe. In one aspect, the reactionmixture includes a probe with a target hybridizing sequence selectedfrom Tables 1, 2 and/or 3. In one aspect, the reaction mixture is amultiplex reaction mixture and includes at least two primer pairs. Inone aspect, the reaction mixture is a multiplex reaction mixture andincludes at least two primer pairs for amplifying two or more of swineH1N1 influenza A virus, seasonal H1 influenza A virus or seasonal H3influenza A virus. At least one primer member of one of the at least twoprimer pairs is selected from Tables 1, 2 and/or 3. At least one primermember of two of the at least two primer pairs is selected from Tables1, 2 and/or 3. At least one primer member of each of the at least twoprimer pairs is selected from Tables 1, 2, and/or 3. In one aspect, themultiplex reaction mixture includes at least two probes, each having atarget hybridizing sequence selected from Tables 1, 2 and/or 3. Furtherembodiments include methods for detectably amplifying an influenza Avirus using one or more of these oligomers.

Another embodiment is a method of detecting nucleic acid of swine H1N1influenza A virus, seasonal H1 influenza A virus and seasonal H3influenza A virus in a sample, that includes the steps of amplifying atarget sequence in a swine H1N1 influenza A virus nucleic acid, seasonalH1 influenza A virus nucleic acid, and/or seasonal H3 influenza A viruscontained in a sample by using a nucleic acid polymerase in vitro toproduce an amplified product, wherein the target sequence of swine H1N1influenza A virus is contained in the swine H1N1 influenza A virus orthe complete complement thereof, or RNA equivalents thereof, the targetsequence of seasonal H1 influenza A virus is contained in the seasonalinfluenza A virus sequence, or the complete complement thereof or theRNA equivalents thereof, and the target sequence of seasonal H3influenza A virus is contained in seasonal Influenza A virus, sequenceencoding H3, or the complete complement thereof, or the RNA equivalentsthereof, and detecting the amplified product.

A particular embodiment of the method also includes the steps ofproviding an internal control oligomer, amplifying a target sequencecontained in the internal control oligomer, and detecting the amplifiedproduct made from the internal control oligomer, thereby indicating thatthe amplifying and detecting steps of the method are properly performed.In another particular embodiment, the method also isolating an influenzavirus nucleic acid from the sample containing the H1N1 Influenza Avirus, seasonal H1 Influenza A virus, or seasonal H3 Influenza A virusnucleic acid before the amplifying step.

One embodiment is a method for the detection of an influenza A virusfrom a sample, comprising the steps of: contacting an influenza A virusnucleic acid from a sample with a primer composition according to Tables1, 2 and/or 3; providing conditions for amplifying the nucleic acid by apolymerase chain reaction to generate an amplification product from thenucleic acid; and detecting the presence or absence of amplificationproduct, wherein the presence of the amplification product indicatesthat the sample contained an influenza A virus. In one aspect, thedetecting step is a real-time detecting step. In one aspect, thedetecting step is a taqman PCR detecting step. In one aspect, the esample contains an influenza A virus nucleic acid selected from thegroup consisting of: a H1N1 influenza A virus nucleic acid, a seasonalH1 influenza A virus nucleic acid, a seasonal H3 influenza A virus, anda combination thereof. In one aspect, the sample contains an influenza Avirus nucleic acid that is substantially identical to an influenza Avirus selected from the group consisting of: a H1N1 influenza A virusnucleic acid, a seasonal H1 influenza A virus nucleic acid and aseasonal H3 influenza A virus, and an amplification product is generatedtherefrom. In one aspect, the sample contains an influenza A virusnucleic acid that is at least 90% identical to an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid, a seasonal H1 influenza A virus nucleic acid and a seasonal H3influenza A virus, and an amplification product is generated therefrom.In one aspect, the sample contains an influenza A virus nucleic acidthat has an H1 gene that is substantially identical to the H1 gene of aninfluenza A virus selected from the group consisting of: a H1N1influenza A virus nucleic acid and a seasonal H1 influenza A virusnucleic acid, and an amplification product is generated therefrom. Inone aspect, the sample contains an influenza A virus nucleic acid thathas an H1 gene that is at least 90% identical to the H1 gene of aninfluenza A virus selected from the group consisting of: a H1N1influenza A virus nucleic acid and a seasonal H1 influenza A virusnucleic acid, and an amplification product is generated therefrom. Inone aspect, the amplifying step is a multiplex amplification reactionfor detecting two or more of an influenza A virus nucleic acid, each ofwhich are independently at least 90% identical to an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid, a seasonal H1 influenza A virus nucleic acid and a seasonal H3influenza A virus.

One embodiment is a method for the detection of an influenza A virusfrom a sample, comprising the steps of: contacting an influenza A virusnucleic acid from a sample with a composition according to one ofMixture 1 to Mixture 23; providing conditions for amplifying the nucleicacid by a polymerase chain reaction to generate an amplification productfrom the nucleic acid; and detecting the presence or absence ofamplification product, wherein the presence of the amplification productindicates that the sample contained an influenza A virus. In one aspect.the detecting step is a real-time detecting step. In one aspect, thedetecting step is a taqman PCR detecting step. In one aspect, the samplecontains an influenza A virus nucleic acid selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid, a seasonal H1influenza A virus nucleic acid, a seasonal H3 influenza A virus, and acombination thereof, and an amplification product is generatedtherefrom. In one aspect, the sample contains an influenza A virusnucleic acid that is substantially identical to an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid, a seasonal H1 influenza A virus nucleic acid and a seasonal H3influenza A virus, and an amplification product is generated therefrom.In one aspect, the sample contains an influenza A virus nucleic acidthat is at least 90% identical to an influenza A virus selected from thegroup consisting of: a H1N1 influenza A virus nucleic acid, a seasonalH1 influenza A virus nucleic acid and a seasonal H3 influenza A virus,and an amplification product is generated therefrom. In one aspect, thesample contains an influenza A virus nucleic acid that has an H1 genethat is substantially identical to the H1 gene of an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid and a seasonal H1 influenza A virus nucleic acid, and anamplification product is generated therefrom. In one aspect, the samplecontains an influenza A virus nucleic acid that has an H1 gene that isat least 90% identical to the H1 gene of an influenza A virus selectedfrom the group consisting of: a H1N1 influenza A virus nucleic acid anda seasonal H1 influenza A virus nucleic acid, and an amplificationproduct is generated therefrom. in one aspect, the amplifying step is amultiplex amplification reaction for detecting two or more of aninfluenza A virus nucleic acid, each of which are independently at least90% identical to an influenza A virus selected from the group consistingof: a H1N1 influenza A virus nucleic acid, a seasonal H1 influenza Avirus nucleic acid and a seasonal H3 influenza A virus, and anamplification product is generated therefrom.

One embodiment is a method for the detection of an H1N1 Influenza AVirus from a sample, comprising the steps of: contacting an H1N1Influenza A Virus from a sample with primer pair selected from Table 1;providing conditions for amplifying the nucleic acid by a polymerasechain reaction to generate an amplification product from the nucleicacid; and detecting the presence or absence of amplification product,wherein the presence of the amplification product indicates that thesample contained an H1N1 Influenza A Virus. In one aspect, the detectingstep is a real-time detecting step. in one aspect, the detecting step isa taqman PCR detecting step. In one aspect, the detecting step uses aprobe selected from Table 1. In one aspect, the sample further containsan influenza A virus nucleic acid selected from the group consisting of:a seasonal H1 influenza A virus nucleic acid, a seasonal H3 influenza Avirus, and a combination thereof, and an amplification product isgenerated therefrom. In one aspect, the amplifying step is a multiplexamplification reaction that further comprises a primer pair from Table2, a primer pair from Table 3 or a primer pair from Table 2 and a primerpair from Table 3. In one aspect, the detecting step further comprises aprobe from Table 2, a probe from Table 3 or a probe from Table 2 and aprobe from Table 3. In one aspect, the amplifying step generates adetectable amplification product from an influenza A virus nucleic acidthat is at least 90% identical to an influenza A virus nucleic acidselected from the group consisting of: an H1N1 influenza virus nucleicacid, a seasonal H1 influenza A virus nucleic acid, a seasonal H3influenza A virus, and a combination thereof. in one aspect, theamplification product is detected using a taqman probe having a nucleicacid sequence according to a probe sequence in Table 2 or Table 3.

One embodiment is a method for the detection of a seasonal H1 InfluenzaA Virus from a sample, comprising the steps of: contacting a seasonal H1Influenza A Virus nucleic acid from a sample with primer pair selectedfrom Table 2; providing conditions for amplifying the nucleic acid by apolymerase chain reaction to generate an amplification product from thenucleic acid; and detecting the presence or absence of amplificationproduct, wherein the presence of the amplification product indicatesthat the sample contained a seasonal H1 Influenza A Virus. In oneaspect, the detecting step is a real-time detecting step. In one aspect,the detecting step is a taqman PCR detecting step. in one aspect, thedetecting step uses a probe selected from Table 2. In one aspect, thesample further contains an influenza A virus nucleic acid selected fromthe group consisting of: a H1N1 influenza A virus nucleic acid, aseasonal H3 influenza A virus, and a combination thereof, and anamplification product is generated therefrom. In one aspect, theamplifying step is a multiplex amplification reaction that furthercomprises a primer pair from Table 1, a primer pair from Table 3 or aprimer pair from Table 1 and a primer pair from Table 3. in one aspect,the detecting step further comprises a probe from Table 1, a probe fromTable 3 or a probe from Table 1 and a probe from Table 3. in one aspect,the amplifying step generates a detectable amplification product from aninfluenza A virus nucleic acid that is at least 90% identical to aninfluenza A virus nucleic acid selected from the group consisting of: aH1N1 influenza A virus nucleic acid, a seasonal H3 influenza A virus,and a combination thereof.

One embodiment is a method for the detection of a seasonal H3 InfluenzaA Virus from a sample, comprising the steps of: contacting a seasonal H3Influenza A Virus nucleic acid from a sample with primer pair selectedfrom Table 3; providing conditions for amplifying the nucleic acid by apolymerase chain reaction to generate an amplification product from thenucleic acid; and detecting the presence or absence of amplificationproduct, wherein the presence of the amplification product indicatesthat the sample contained a seasonal H3 Influenza A Virus. In one aspectthe detecting step is a real-time detecting step. in one aspect, thedetecting step is a taqman PCR detecting step. In one aspect, thedetecting step uses a probe selected from Table 3. In one aspect, thesample further contains an influenza A virus nucleic acid selected fromthe group consisting of: a H1N1 influenza A virus nucleic acid, aseasonal H1 influenza A virus, and a combination thereof, and anamplification product is generated therefrom. In one aspect, theamplifying step is a multiplex amplification reaction that furthercomprises a primer pair from Table 1, a primer pair from Table 2 or aprimer pair from Table 1 and a primer pair from Table 2. In one aspect,the detecting step further comprises a probe from Table 1, a probe fromTable 2 or a probe from Table 1 and a probe from Table 2. In one aspect,the amplifying step generates a detectable amplification product from aninfluenza A virus nucleic acid that is at least 90% identical to aninfluenza A virus nucleic acid selected from the group consisting of: aH1N1 influenza A virus nucleic acid, a seasonal H1 influenza A virus, aseasonal H3 influenza A virus, and a combination thereof.

One embodiment of the methods further provides a separating step whereinnucleic acids are removed from one or more other components in thesample. in one aspect, the separating step takes place before theamplifying step. In one aspect, the separating step is performed using atarget capture oligomer having a tail selected from the group consistingof dT₀₋₃dA₁₂₋₃₀, and using a solid support having an immobilized probethat is substantially complementary to the tail. In one aspect, theseparating step is a non-specific separating step. In one aspect, thenon-specific separating step is performed by adhering nucleic acidsreversibly to a solid support, followed by washing and elution of theadhered nucleic acids into a substantially aqueous solution (e.g., usinga MagNA Pure LC System (Roche) and the MagNA Pure Total Nucleic AcidIsolation Kit (Roche) or a NucliSENS easy MAG System (bioMériuex and theAutomated Magnetic Extraction Reagents (bioMérieux), or using anon-specific target capture probe (WO 2008/016988) or comparable nucleicacid extraction instrument(s) and/or reagent kit(s))

DETAILED DESCRIPTION

In one aspect, the present invention involves performing anamplification reaction. Preferably, the amplification reaction is a PCRreaction. However, there are other suitable amplification techniquessuch as CPR (Cycling Probe Reaction), bDNA (Branched DNA Amplification),SSR (Self-Sustained Sequence Replication), SDA (Strand DisplacementAmplification), QBR (Q-Beta Replicase), Re-AMP (Formerly RAMP), NASBA(Nucleic Acid Sequence Based Amplification), RCR (Repair ChainReaction), LCR (Ligase Chain Reaction), TAS (Transorbtion BasedAmplification System), HCS (amplified ribosomal RNA), and TMA(Transcription Mediated Amplification).

The disclosed nucleic acid sequences and methods are useful foramplifying and detecting swine H1N1 influenza A virus, seasonal H1influenza A virus, and/or seasonal H3 influenza A virus nucleic acidsfrom viral particles present in a sample in a relatively short time sothat diagnosis can be made during early stages of infection (e.g.,within 48 hr of symptoms) and effective treatment can be initiated. Themethods are useful for screening for individuals who have influenzavirus infections but who do not exhibit definitive symptoms,particularly for screening patients who have a higher risk of death orserious complications from influenza virus infections, e.g., young,elderly, or immuno-compromised individuals. The methods are furtheruseful for identifying influenza type that is causing an infection sothat a proper course of treatment can be applied. The methods are alsouseful for rapid screening of many samples, such as during an epidemicor pandemic, so that appropriate public health responses can beinitiated. The methods are useful because they minimize the risk ofexposure of laboratory personnel to infectious agents, such as an avianinfluenza virus related to swine H1N1 influenza A virus, seasonal H1influenza A virus, and/or seasonal H3 influenza A virus that have becomeinfectious to humans. Thus, the methods and compositions disclosedherein respond to a need for rapid, sensitive, and specific testing ofclinical samples that may contain swine H1N1 influenza A virus, seasonalH1 influenza A virus, and/or seasonal H3 influenza A virus.

DEFINITIONS

Seasonal H1 Influenza A includes various strains of Influenza A whichhave the H1 subtype. Sequences specific for the seasonal H1 Influenza Amay be identical to a portion of a single strain or may be a consensussequence shared between multiple strains. However, to ensure thatmultiple strains of the seasonal H1 Influenza A virus are detected usingthe claimed compositions, kits, and methods, the sequences used asprimers and probes were designed from regions of the genome that aregenerally conserved among many strains of seasonal H1 Influenza A virus.

Seasonal H3 Influenza A virus includes various strains of Influenza Awhich have the H3 subtype. To ensure that multiple strains of theseasonal H3 Influenza A virus are detected using the claimedcompositions, kits, and methods, the sequences specific for H3 influenzaA virus that were used as primers and probes were designed for regionsof the genome that are generally conserved among many strains ofseasonal H3 Influenza A virus.

The swine H1N1 influenza A virus, when referred to as such, is areassortment virus composed of at least two genes from one or moreinfluenza viruses that normally circulate in swine in Europe and Asia,in addition to bird (avian) and human genes. The 2009 swine H1N1influenza A virus is also considered a swine H1N1 influenza A virus.Sequences specific for the swine H1N1 influenza A virus may represent aconsensus sequence between multiple strains or occurrences. To ensurethat multiple strains of the swine H1N1 influenza A virus are detectedusing the claimed and/or disclosed compositions, kits, reaction mixturesand methods, the sequences used as primers and probes were designed fromregions of the genome that are conserved among many strains of the swineH1N1 influenza A virus, but that are not conserved in the seasonal H1influenza A or seasonal H3 influenza A viral sequences.

A “sample” or “specimen”, including “biological” or “clinical” samples,refers to a tissue or material derived from a living or dead human oranimal which may contain an influenza virus target nucleic acid,including, for example, nasopharyngeal or throat swabs, nasal orbronchial washes, nasal aspirates, sputum, other respiratory tissue orexudates, biopsy tissue including lymph nodes, or body fluids such asblood or urine. A sample may be treated to physically or mechanicallydisrupt tissue or cell structure to release intracellular nucleic acidsinto a solution which may contain enzymes, buffers, salts, detergentsand the like, to prepare the sample for analysis.

“Nucleic acid” refers to a multimeric compound comprising nucleosides ornucleoside analogs which have nitrogenous heterocyclic bases or baseanalogs linked together to form a polynucleotide, including conventionalRNA, DNA, mixed RNA-DNA, and polymers that are analogs thereof. Anucleic acid “backbone” may be made up of a variety of linkages,including one or more of sugar-phosphodiester linkages, peptide-nucleicacid bonds (“peptide nucleic acids” or PNA; PCT No. WO 95/32305),phosphorothioate linkages, methylphosphonate linkages, or combinationsthereof. Sugar moieties of a nucleic acid may be ribose, deoxyribose, orsimilar compounds with substitutions, e.g., 2′ methoxy or 2′ halidesubstitutions. Nitrogenous bases may be conventional bases (A, G, C, T,U), analogs thereof (e.g., inosine or others; see The Biochemistry ofthe Nucleic Acids 5-36, Adams et al., ed., 11^(th) ed., 1992),derivatives of purines or pyrimidines (e.g., N⁴-methyl deoxygaunosine,deaza- or aza-purines, deaza- or aza-pyrimidines, pyrimidine bases withsubstituent groups at the 5 or 6 position, purine bases with asubstituent at the 2, 6 or 8 positions, 2-amino-6-methylaminopurine,O⁶-methylguanine, 4-thio-pyrimidines, 4-amino-pyrimidines,4-dimethylhydrazine-pyrimidines, and O⁴-alkyl-pyrimidines; U.S. Pat. No.5,378,825 and PCT No. WO 93/13121). Nucleic acids may include one ormore “abasic” residues where the backbone includes no nitrogenous basefor position(s) of the polymer (U.S. Pat. No. 5,585,481). A nucleic acidmay comprise only conventional RNA or DNA sugars, bases and linkages, ormay include both conventional components and substitutions (e.g.,conventional bases with 2′ methoxy linkages, or polymers containing bothconventional bases and one or more base analogs). Nucleic acid includes“locked nucleic acid” (LNA), an analogue containing one or more LNAnucleotide monomers with a bicyclic furanose unit locked in an RNAmimicking sugar conformation, which enhance hybridization affinitytoward complementary RNA and DNA sequences (Vester and Wengel, 2004,Biochemistry 43(42):13233-41). Embodiments of oligomers that may affectstability of a hybridization complex include PNA oligomers, oligomersthat include 2′-methoxy or 2′-fluoro substituted RNA, or oligomers thataffect the overall charge, charge density, or steric associations of ahybridization complex, including oligomers that contain charged linkages(e.g., phosphorothioates) or neutral groups (e.g., methylphosphonates).

By “RNA and DNA equivalents” is meant RNA and DNA molecules havingessentially the same complementary base pair hybridization properties.RNA and DNA equivalents have different sugar moieties (i.e., riboseversus deoxyribose) and may differ by the presence of uracil in RNA andthymine in DNA. The differences between RNA and DNA equivalents do notcontribute to differences in homology because the equivalents have thesame degree of complementarity to a particular sequence.

An “oligomer” or “oligonucleotide” refers to a nucleic acid of generallyless than 1,000 nucleotides (nt), including those in a size range havinga lower limit of about 2 to 5 nt and an upper limit of about 500 to 900nt. Some particular embodiments are oligomers in a size range with alower limit of about 5 to 15, 16, 17, 18, 19, or 20 nt and an upperlimit of about 50 to 600 nt, and other particular embodiments are in asize range with a lower limit of about 10 to 20 nt and an upper limit ofabout 22 to 100 nt. Oligomers may be purified from naturally occurringsources, but preferably are synthesized by using any well knownenzymatic or chemical method. Oligomers may be referred to by afunctional name (e.g., capture probe, primer or promoter primer) butthose skilled in the art will understand that such terms refer tooligomers.

By “antisense,” “opposite sense,” or “negative sense” is meant a nucleicacid molecule completely complementary to a reference, or sense, nucleicacid molecule.

By “sense,” “same-sense” or “positive sense” is meant a nucleic acidmolecule perfectly homologous to a reference nucleic acid molecule.

By “amplicon” or “amplification product” is meant a nucleic acidmolecule generated in a nucleic acid amplification reaction and which isderived from a target nucleic acid. An amplicon or amplification productcontains a target nucleic acid sequence that may be of the same oropposite sense as the target nucleic acid.

An “immobilized probe”, “immobilized oligomer” or “immobilized nucleicacid” refers to a nucleic acid binding partner that joins a captureoligomer to a support, directly or indirectly. An immobilized probejoined to a support facilitates separation of a capture probe boundtarget from unbound material in a sample. The immobilized probehybridizes with the immobilized probe binding region of the captureprobe, thereby forming an immobilized probe:capture probe complex. Inthe presence of a target nucleic acid, an immobilized probe:captureprobe:target nucleic acid complex forms. Any support may be used, e.g.,matrices or particles free in solution, which may be made of any of avariety of materials, e.g., nylon, nitrocellulose, glass, polyacrylate,mixed polymers, polystyrene, silane polypropylene, or metal. Targetcapture reagents may optionally include imidazoleum compounds, urea andthe like (e.g., WO 2006/121888). Particular embodiments use a supportthat is magnetically attractable particles, e.g., monodisperseparamagnetic beads (uniform size±5%) to which an immobilized probe isjoined directly (e.g., via covalent linkage, chelation, or ionicinteraction) or indirectly (e.g., via a linker), where the joining isstable during nucleic acid hybridization conditions.

“Capture-probe,” “target capture probe” or “target capture oligomer”refers to a nucleic acid oligomer that is used to separate nucleic acidsin a sample from other components of the sample. Typically, the targetcapture oligomer has at least two regions: the target-hybridizingregion; and the binding-pair region, usually on the same oligomer,although the two regions may be present on two different oligomersjoined together by one or more linkers. The binding-pair region issometimes referred to as a tail portion of the capture probe. Thetarget-hybridizing region is a contiguous nucleic acid sequence that isconfigured to hybridize to nucleic acids in the sample. Thetarget-hybridizing region can be configured to specifically hybridize toa particular nucleic acid species in a group of nucleic acids. In thisinstance, the target-hybridizing region is configured to besubstantially complementary to a given sequence on a particular nucleicacid species. The target-hybridizing region can be configured tospecifically hybridize to a subset of nucleic acid species in a group ofnucleic acids, wherein the subset share a similar nucleic acid sequenceat at least part of their overall sequences. In this instance, thetarget-hybridizing region is configured to be substantiallycomplementary to this shared similar sequence on these subset of nucleicacid species. The target-hybridizing region can also be configured tonon-specifically hybridize to nucleic acids in a group of nucleic acids(WO 2008/016988). In this instance, the target-hybridizing region is notconfigured to be substantially complementary to any given sequence on aparticular nucleic acid species. Rather, the target-hybridizing sequencecan be configured to generally hybridize with nucleic acids in a group.Non-specific target capture is designed to separate nucleic acids in asample from the non-nucleic acid components, whereas specific targetcapture is designed to separate a particular species or subset ofnucleic acids from other nucleic acids and non-nucleic acids in asample. The binding pair portion of the target capture oligomer isconfigured to join with a complementary binding pair; typically presenton a solid support. When the binding pair portion of the target captureoligomer is itself a nucleic acid sequence, then the complementarybinding pair on a solid support is a nucleic acid with a substantiallycomplementary nucleic acid sequence (also referred to as an immobilizedprobe). Commonly, the binding pair portion of a target capture oligomeris a substantially homopolymeric nucleic acid sequence (e.g., a poly dTand/or a poly dA nucleic acid sequence). In this instance, then, theimmobilized probe is a substantially complementary nucleic acid. Onecommon example is a target capture oligomer having a binding pair regionthat is a dA₀₋₃dT₁₂₋₃₀ nucleic acid sequence. In this instance, theimmobilized probe would then be a substantially complementary nucleicacid sequence (e.g., dA₀₋₃dT₁₂₋₃₀). Additionally, a nucleic acidbinding-pair region of a capture probe is often made so to not bindnucleic acids in the sample by, for example, giving the nucleic acids aleft-handed chirality. In this instance, the immobilized probe is alsomade left-handed. Thus, the binding pair region and the immobilizedprobe do not bind nucleic acids in the sample because of the oppositechirality. Other examples of binding pair regions/complementary bindingpairs that can be used include; (a) a receptor and ligand pair, (b) anenzyme and substrate pair, (c) an enzyme and cofactor pair, (d) anenzyme and coenzyme pair, (e) an antibody and antigen pair, (f) anantibody fragment and antigen pair, (g) a sugar and lectin pair, (h) aligand and chelating agent pair, (i) biotin and avidin, (j) biotin andstreptavidin, and (k) nickel and histidine.

“Separating” or “purifying” refers to removing one or more components ofa sample from one or more other sample components, e.g., removing somenucleic acids from a generally aqueous solution that may also containproteins, carbohydrates, lipids, or other nucleic acids. In particularembodiments, a separating or purifying step removes the target nucleicacid from at least about 70%, more preferably at least about 90% and,even more preferably, at least about 95% of the other sample components.

An “amplification oligonucleotide” or “amplification oligomer” refers toan oligonucleotide that hybridizes to a target nucleic acid, or itscomplement, and participates in a nucleic acid amplification reaction,e.g., serving as a primer or and promoter-primer. Particularamplification oligomers contain at least about 10 contiguous bases, andmore preferably at least 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20contiguous bases, that are complementary to a region of the targetnucleic acid sequence or its complementary strand. The contiguous basesare preferably at least about 80%, more preferably at least about 90%,and most preferably completely complementary to the target sequence towhich the amplification oligomer binds. One skilled in the art willunderstand that the recited ranges include all whole and rationalnumbers within the range (e.g., 92% or 98.377%). Particularamplification oligomers are about 10 to about 60 bases long andoptionally may include modified nucleotides.

A “primer” refers to an oligomer that hybridizes to a template nucleicacid and has a 3′ end that is extended by polymerization. A primer maybe optionally modified, e.g., by including a 5′ region that isnon-complementary to the target sequence. Such modification can includefunctional additions, such as tags, promoters or other sequences used oruseful for manipulating or amplifying the primer or targetoligonucleotide.

Within the context of transcription mediated amplification, a primermodified with a 5′ promoter sequence may be referred to as a“promoter-primer.” A person of ordinary skill in the art of molecularbiology or biochemistry will understand that an oligomer that canfunction as a primer can be modified to include a 5′ promoter sequenceand then function as a promoter-primer, and, similarly, anypromoter-primer can serve as a primer with or without its 5′ promotersequence.

“Nucleic acid amplification” refers to any well known in vitro procedurethat produces multiple copies of a target nucleic acid sequence, or itscomplementary sequence, or fragments thereof (i.e., an amplifiedsequence containing less than the complete target nucleic acid).Examples of well known nucleic acid amplification procedures includetranscription associated methods, such as transcription-mediatedamplification (TMA), nucleic acid sequence-based amplification (NASBA)and others (e.g., U.S. Pat. Nos. 5,399,491, 5,554,516, 5,437,990,5,130,238, 4,868,105, and 5,124,246), replicase-mediated amplification(e.g., U.S. Pat. No. 4,786,600), the polymerase chain reaction (PCR)(e.g., U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159), ligase chainreaction (LCR) (e.g., EP Pat. App. 0320308) and strand-displacementamplification (SDA) (e.g., U.S. Pat. No. 5,422,252). Replicase-mediatedamplification uses self-replicating RNA molecules, and a replicase suchas QB-replicase. PCR amplification uses DNA polymerase, primers, andthermal cycling steps to synthesize multiple copies of the twocomplementary strands of DNA or cDNA. LCR amplification uses at leastfour separate oligonucleotides to amplify a target and its complementarystrand by using multiple cycles of hybridization, ligation, anddenaturation. SDA uses a primer that contains a recognition site for arestriction endonuclease that will nick one strand of a hemimodified DNAduplex that includes the target sequence, followed by amplification in aseries of primer extension and strand displacement steps. Particularembodiments use PCR or TMA, but it will be apparent to persons ofordinary skill in the art that oligomers disclosed herein may be readilyused as primers in other amplification methods.

Transcription associated amplification uses a DNA polymerase, an RNApolymerase, deoxyribonucleoside triphosphates, ribonucleosidetriphosphates, a promoter-containing oligonucleotide, and optionally mayinclude other oligonucleotides, to ultimately produce multiple RNAtranscripts from a nucleic acid template (described in detail in U.S.Pat. Nos. 5,399,491 and 5,554,516, Kacian et al., U.S. Pat. No.5,437,990, Burg et al., PCT Nos. WO 88/01302 and WO 88/10315, Gingeraset al., U.S. Pat. No. 5,130,238, Malek et al., U.S. Pat. Nos. 4,868,105and 5,124,246, Urdea et al., PCT No. WO 94/03472, McDonough et al., PCTNo. WO 95/03430, and Ryder et al.). Methods that use TMA are describedin detail previously (U.S. Pat. Nos. 5,399,491 and 5,554,516).

In methods that detect amplification products in real-time, the term“Threshold cycle” (Ct) is a measure of the emergence time of a signalassociated with amplification of target, and is generally 10× standarddeviation of the normalized reporter signal. Once an amplificationreaches the “threshold cycle”, generally there is considered to be apositive amplification product of a sequence to which the probe binds.The identity of the amplification product can then be determined throughmethods known to one of skill in the art, such as gel electrophoresis,nucleic acid sequencing, and other such well known methods.

As used herein, the term “relative fluorescence unit” (“RFU”) is a unitof measurement of fluorescence intensity. RFU varies with thecharacteristics of the detection means used for the measurement, and canbe used as a measurement to compare relative intensities between samplesand controls. The analytical sensitivity (limit of detection or LoD) isdetermined from the median tissue culture infective dose (TCID₅₀/ml).The TCID₅₀/ml is that amount of a pathogenic agent that will producepathological change in 50% of cell cultures inoculated.

“Detection probe” refers to a nucleic acid oligomer that hybridizesspecifically to a target sequence, including an amplified sequence,under conditions that promote nucleic acid hybridization, for detectionof the target nucleic acid. Detection may either be direct (i.e., probehybridized directly to the target) or indirect (i.e., a probe hybridizedto an intermediate structure that links the probe to the target). Aprobe's target sequence generally refers to the specific sequence withina larger sequence which the probe hybridizes specifically. A detectionprobe may include target-specific sequences and anon-target-complementary sequence. Such non-target-complementarysequences can include sequences which will confer a desired secondary ortertiary structure, such as a hairpin structure, which can be used tofacilitate detection and/or amplification. (e.g., U.S. Pat. Nos.5,118,801, 5,312,728, 6,835,542, and 6,849,412). Probes of a definedsequence may be produced by techniques known to those of ordinary skillin the art, such as by chemical synthesis, and by in vitro or in vivoexpression from recombinant nucleic acid molecules.

By “hybridization” or “hybridize” is meant the ability of two completelyor partially complementary nucleic acid strands to come together underspecified hybridization assay conditions in a parallel or preferablyantiparallel orientation to form a stable structure having adouble-stranded region. The two constituent strands of thisdouble-stranded structure, sometimes called a hybrid, are held togetherby hydrogen bonds. Although these hydrogen bonds most commonly formbetween nucleotides containing the bases adenine and thymine or uracil(A and T or U) or cytosine and guanine (C and G) on single nucleic acidstrands, base pairing can also form between bases which are not membersof these “canonical” pairs. Non-canonical base pairing is well-known inthe art. (See, e.g., R. L. P. Adams et al., The Biochemistry of theNucleic Acids (11.sup.th ed. 1992).)

By “preferentially hybridize” is meant that under stringenthybridization conditions, an amplification or detection probe oligomercan hybridize to its target nucleic acid to form stable oligomer:targethybrid, but not form a sufficient number of stable oligomer:non-targethybrids. Amplification and detection oligomers that preferentiallyhybridize to a target nucleic acid are useful to amplify and detecttarget nucleic acids, but not non-targeted organisms, especiallyphylogenetically closely related organisms. Thus, the oligomerhybridizes to target nucleic acid to a sufficiently greater extent thanto non-target nucleic acid to enable one having ordinary skill in theart to accurately amplify and/or detect the presence (or absence) ofnucleic acid derived from the specified influenza viruses asappropriate. In general, reducing the degree of complementarity betweenan oligonucleotide sequence and its target sequence will decrease thedegree or rate of hybridization of the oligonucleotide to its targetregion. However, the inclusion of one or more non-complementarynucleosides or nucleobases may facilitate the ability of anoligonucleotide to discriminate against non-target organisms.

Preferential hybridization can be measured using techniques known in theart and described herein, such as in the examples provided below.Preferably, there is at least a 10-fold difference between target andnon-target hybridization signals in a test sample, more preferably atleast a 100-fold difference, and most preferably at least a 1,000-folddifference. Preferably, non-target hybridization signals in a testsample are no more than the background signal level.

By “stringent hybridization conditions,” or “stringent conditions” ismeant conditions permitting an oligomer to preferentially hybridize to atarget nucleic acid (preferably an HA, NA or NP gene or transcripttherefrom derived from one or more virus strains of the specifiedinfluenza A virus types) and not to nucleic acid derived from a closelyrelated non-target nucleic acids. Stringent hybridization conditions mayvary depending upon factors including the GC content and length of theoligomer, the degree of similarity between the oligomer sequence andsequences of non-target nucleic acids that may be present in the testsample, and the target sequence. Hybridization conditions include thetemperature and the composition of the hybridization reagents orsolutions. Preferred hybridization assay conditions for amplifyingand/or detecting target nucleic acids derived from one or more virusstrains of the specified influenza A virus types with the probes of thepresent invention correspond to a temperature of about 60° C. when thesalt concentration is in the range of about 0.6-0.9 M. Specifichybridization assay conditions are set forth infra in the Examplessection. Other acceptable stringent hybridization conditions could beeasily ascertained by those having ordinary skill in the art.

By “assay conditions” is meant conditions permitting stablehybridization of an oligonucleotide to a target nucleic acid. Assayconditions do not require preferential hybridization of theoligonucleotide to the target nucleic acid.

“Label” or “detectable label” refers to a moiety or compound joineddirectly or indirectly to a probe that is detected or leads to adetectable signal. Direct joining may use covalent bonds or non-covalentinteractions (e.g., hydrogen bonding, hydrophobic or ionic interactions,and chelate or coordination complex formation) whereas indirect joiningmay use a bridging moiety or linker (e.g., via an antibody or additionaloligonucleotide(s), which amplify a detectable signal. Any detectablemoiety may be used, e.g., radionuclide, ligand such as biotin or avidin,enzyme, enzyme substrate, reactive group, chromophore such as a dye orparticle (e.g., latex or metal bead) that imparts a detectable color,luminescent compound (e.g. bioluminescent, phosphorescent orchemiluminescent compound), and fluorescent compound (i.e.,fluorophore). Embodiments of fluorophores include those that absorblight in the range of about 495 to 650 nm and emit light in the range ofabout 520 to 670 nm, which include those known as FAM™, TET™, CAL FLUOR™(Orange or Red), and QUASAR™ compounds. Fluorophores may be used incombination with a quencher molecule that absorbs light when in closeproximity to the fluorophore to diminish background fluorescence. Suchquenchers are well known in the art and include, e.g., BLACK HOLEQUENCHER™ (or BHQ™) or TAMRA™ compounds. Particular embodiments includea “homogeneous detectable label” that is detectable in a homogeneoussystem in which bound labeled probe in a mixture exhibits a detectablechange compared to unbound labeled probe, which allows the label to bedetected without physically removing hybridized from unhybridizedlabeled probe (e.g., U.S. Pat. Nos. 5,283,174, 5,656,207 and 5,658,737).Particular homogeneous detectable labels include chemiluminescentcompounds, more preferably acridinium ester (“AE”) compounds, such asstandard AE or AE derivatives which are well known (U.S. Pat. Nos.5,656,207, 5,658,737, and 5,639,604). Methods of synthesizing labels,attaching labels to nucleic acid, and detecting signals from labels arewell known (e.g., Sambrook et al., Molecular Cloning, A LaboratoryManual, 2nd ed. (Cold Spring Harbor Laboratory Press, Cold SpringHarbor, N. Y., 1989) at Chapt. 10, and U.S. Pat. Nos. 5,658,737,5,656,207, 5,547,842, 5,283,174, and 4,581,333, and EP Pat. App. 0 747706). Particular methods of linking an AE compound to a nucleic acid areknown (e.g., U.S. Pat. No. 5,585,481 and U.S. Pat. No. 5,639,604, seecolumn 10, line 6 to column 11, line 3, and Example 8). Particular AElabeling positions are a probe's central region and near a region of A/Tbase pairs, at a probe's 3′ or 5′ terminus, or at or near a mismatchsite with a known sequence that is the probe should not detect comparedto the desired target sequence. Other detectably labeled probes includeTaqMan probes, molecular torches and molecular beacons. TaqMan probesinclude a donor and acceptor label wherein fluorescence is detected uponenzymatically degrading the probe during amplification in order torelease the fluorophore from the presence of the quencher. Moleculartorches and beacons exist in open and closed configurations wherein theclosed configuration quenches the fluorophore and the open positionseparates the fluorophore from the quencher to allow fluorescence.Hybridization to target opens the otherwise closed probes.

Sequences are “sufficiently complementary” if they allow stablehybridization of two nucleic acid sequences, e.g., stable hybrids ofprobe and target sequences, although the sequences need not becompletely complementary. That is, a “sufficiently complementary”sequence that hybridizes to another sequence by hydrogen bonding betweena subset series of complementary nucleotides by using standard basepairing (e.g., G:C, A:T or A:U), although the two sequences may containone or more residues (including abasic positions) that are notcomplementary so long as the entire sequences in appropriatehybridization conditions to form a stable hybridization complex.Sufficiently complementary sequences are preferably at least about 80%,more preferably at least about 90%, and most preferably completelycomplementary in the sequences that hybridize together. Appropriatehybridization conditions are well known to those skilled in the art, canbe predicted based on sequence composition, or can be determinedempirically by using routine testing (e.g., Sambrook et al., MolecularCloning, A Laboratory Manual, 2^(nd) ed. at §§1.90-1.91, 7.37-7.57,9.47-9.51 and 11.47-11.57, particularly §§9.50-9.51, 11.12-11.13,11.45-11.47 and 11.55-11.57).

“Consisting essentially of” means that additional component(s),composition(s) or method step(s) that do not materially change the basicand novel characteristics of the compositions and methods describedherein may be included in those compositions or methods. Suchcharacteristics include the ability to detect an influenza virus Anucleic acid sequence present in a sample with specificity thatdistinguishes the influenza virus nucleic acid from at least 50 otherknown respiratory pathogens, preferably at a sensitivity that detects atleast 1.7 to 2.7 log copies of the influenza virus, within about 45 minfrom the beginning of an amplification reaction that makes amplifiedviral sequences that are detected.

Unless defined otherwise, all scientific and technical terms used hereinhave the same meaning as commonly understood by those skilled in therelevant art. General definitions may be found in technical booksrelevant to the art of molecular biology, e.g., Dictionary ofMicrobiology and Molecular Biology, 2nd ed. (Singleton et al., 1994,John Wiley & Sons, New York, N.Y.) or The Harper Collins Dictionary ofBiology (Hale & Marham, 1991, Harper Perennial, New York, N.Y.). Unlessmentioned otherwise, techniques employed or contemplated herein arestandard methodologies well known to one of ordinary skill in the art.The examples included herein illustrate some particular embodiments.

DESCRIPTION

Compositions that include nucleic acid oligomers that function in targetcapture, amplification, and detection of nucleic acids and methods fordetecting swine H1N1 influenza A virus, seasonal H1 influenza A virusand/or seasonal H3 influenza A virus nucleic acids present in abiological sample are disclosed herein.

To select target sequences appropriate for use in the tests to detectswine H1N1 influenza A virus, known swine H1N1 influenza A virus RNA orDNA sequences that encode either the H1 antigen from the swine H1N1influenza A virus or the NP protein from the swine H1N1 influenza Avirus, including partial or complementary sequences (available atpublicly accessible databases, e.g., GenBank), are aligned by matchingregions of identical or similar sequences and compared. Once thesequence homology among the multiple strains is determined, sequencesare chosen for areas which have a high homology among the many strainsof swine H1N1 influenza A virus, and primers and probes are designedaccording to conventional primer and probe design methods. It isimportant to note, however, that because viruses have a high mutationrate, on occasion the conventional tenets of primer and probe design arecompromised on. The primers and probes are then tested against a targetnucleic acid under standard reaction conditions to determine reactivityand specificity. If the probes and primers are not effective against thetarget sequence in singleplex mode, they are not chosen for furthertesting. Effectiveness is determined by the sensitivity of theoligonucleotides and the specificity of the oligonucleotides. Thesequences which are effective in singleplex mode are subsequently testedin a multiplex assay, which included an Internal Control sequence,primers and probe(s). Various target sequences representing multipleswine H1N1 influenza A strains may be tested in singleplex and/ormultiplex mode.

Target sequences appropriate for use in detecting the swine H1N1influenza A virus are preferably not complementary to sequences in theseasonal H1 Influenza A virus or the seasonal H3 Influenza A virus, sothat a positive detection of the swine H1N1 influenza A target sequenceis specific to the swine H1N1 influenza A virus and do not also detectthe other virus types.

In particular, oligonucleotides target the H1 nucleic acid in theregions corresponding to nucleotides 71-244, 316-408, 445-621, 722-868,921-1121, 1215-1407, or 1525-1669 of GenBank Sequence GU984417.1 versionGI:290873747 submitted Mar. 10, 2010 (SEQ ID NO:103), are chosen asprimers and probes. Alternatively, oligonucleotides from the sequenceencoding the NP protein in the regions corresponding to nucleotides38-272, 272-413, 459-648, 768-912, 969-1061, or 1190-1328, of599:A/Thailand/CU-B5/2009(SEQ ID NO:104) are chosen as primers andprobes.

Although oligonucleotides were selected from “regions corresponding to”a single viral nucleic acid sequence, the invention is not limited tooligonucleotides target only the referenced specific sequences or to theparticular cited virus strains. It will be understood by those skilledin the art in possession of this disclosure how to align and determinecorresponding regions between various strains of swine H1N1 influenza Avirus, seasonal H1 influenza A virus and/or seasonal H3 influenza Avirus. In addition, useful primers and probes are not limited to thespecific sequences listed herein, but may have 1, 2, 3, 4, 5, 6, 7, or 8nucleotide substitutions within the conserved region when compared withthe database sequence.

To select target sequences appropriate for use in the tests to detectthe seasonal H1 Influenza virus A, seasonal H1 Influenza virus A RNA orDNA sequences that encode a the H1 antigen, including partial orcomplementary sequences (available at publicly accessible databases,e.g., GenBank) are aligned by matching regions of identical or similarsequences and compared. Similarly, to select target sequencesappropriate for use in the tests to detect the seasonal H3 Influenzavirus A, seasonal H3 Influenza virus A RNA or DNA sequences that encodea the H3 antigen, including partial or complementary sequences(available at publicly accessible databases, e.g., GenBank) are alignedby matching regions of identical or similar sequences and compared. Aswith the swine H1N1 influenza A virus sequences, the primers and probesfor the seasonal H1 Influenza A or seasonal H3 Influenza A are selectedfrom regions having high homology among the various strains of seasonalH1 Influenza A or seasonal H3 Influenza A viruses. The primers andprobes are tested in singleplex then multiplex modes. As with the swineH1N1 influenza A virus primers and probes, the seasonal flu primers andprobes are tested against multiple strains of seasonal H1 Influenza Avirus and seasonal H3 Influenza A virus.

In particular, oligonucleotides from DNA that encodes the H1 antigen ofthe seasonal H1 Influenza A virus in the regions corresponding tonucleotides 658-785, 808-968, 1064-1281 of GenBank Sequence CY030230.1version GI:168805690, submitted May 9, 2008 (SEQ ID NO:105), are chosenas primers and probes for seasonal H1 Influenza A detection. Also,oligonucleotides from the H3 antigen in the regions corresponding tonucleotides 4-179, 157-294, 254-419, 342-510, 632-804, 748-853,841-1084, 886-1085, 1062-1170, 1141-1321, 1281-1389, 1325-1480,1406-1478, or 1488-1668 of GenBank Accession number EU103640.1 versionGI:156691489, submitted Mar. 26, 2008 (SEQ ID NO:106), are chosen asprimers and probes for H3 Influenza A detection.

Although sequence comparisons may be facilitated by use ofcomputer-performed algorithms, one of ordinary skill can perform thecomparisons manually and visually. Portions of sequences for each viraltarget that contained relatively few sequence changes between thecompared individual viral sequences are chosen as a basis for designingsynthetic oligomers for use in the methods described herein.

Exemplary oligonucleotide sequences for detecting the swine H1N1Influenza A target are described in Table 1, exemplary oligomersequences for detecting the seasonal H1 Influenza A Virus target aredescribed in Table 2, and exemplary oligomer sequences for detecting theseasonal H3 Influenza A Virus target are described in Table 3.

Those skilled in the art will recognize that oligomers identified ashaving a preferred function in target capture have target-specificportions and optionally include tail portions which may be deleted orsubstituted with other sequences or binding moieties. Such tail portionsmay be nucleotide or non-nucleotide linkers by which labels or otherancillary molecules used in signaling amplification are attached to theoligonucleotide. For example, for clarity, sequences shown below thatinclude a 5′ fluorophore (“F”) and a 3′ quencher compound (“Q”) arewritten to show the presence of F and Q molecules. Those skilled in theart will appreciate that the ancillary molecules may take many forms,and be placed in many locations in a nucleic acid molecule, such as ateither end or with one or more of the F or Q molecules bound to anucleotide in the middle of the nucleic acid sequence. One of skill inthe art will also recognize that these molecules are not required forthe target specific oligonucleotide to function in embodiments of theclaimed methods or compositions of this application.

TABLE 1  Oligomer Sequences Targeting Swine H1N1 Influenza A VirusPreferred SEQ ID Sequence Function Direction 1 AAGTCGAAACCCAGGAAACPrimer forward 2 CATGCCCACTTGCTACTG Primer reverse 3F-CATACACACAAGCAGGCAGGCA-Q Probe reverse 4 F-AAGACCTCATTTTCCTGGCACGGT-QProbe forward 5 CACGGTCAGCACTCATTC Primer forward 6 TTCAAAGTCATGCCCACTTGPrimer reverse 7 F-ATCAGTTGCACATAAATCCTGCCTG-Q Probe forward 8ATTGGTGGAATCGGGAGATT Primer forward 9 AGGTATTTATTTCTTCTCTCATC Primerreverse 10 F-TCCAAATGTGCACTGAACTCAAACTC-Q Probe forward 11F-TAGTCGTCCATCATAATCACTGAGTTT-Q Probe reverse 12 TGGCGTCTCAAGGCACCPrimer forward 13 TTCCACCAATCATTCTTCCGA Primer reverse 14F-ATCATATGAACAAATGGAGACTGGTGG-Q Probe forward 15F-CGCCAGGATGCCACAGAAATCAGA-Q Probe forward 16F-TGCTCTGATTTCTGTGGCATCCTGG-Q Probe reverse 17 TAGAAGAGCATCCCAGTGCPrimer forward 18 CCATTGTTTGCTTGGCGC Primer reverse 19F-AAGGACCCTAAGAAAACAGGAGGACC-Q Probe forward 20F-TTCTTCTTTGTCATAAAGGATGAGTTCTC-Q Probe reverse 21 CAACCTGAATGATGCCACATPrimer forward 22 TCGGTCATTGATTCCACGTT Primer reverse 23F-AGAGCGCTTGTTCGCACCGGAAT-Q Probe forward 24F-CAGAATGTGCTCTCTAATGCAAGGTTC-Q Probe forward 25F-TCATTCTGATTAACTCCATTGCTATTGTTCC-Q Probe reverse 26 AGTGGTCAGCCTGATGAGAPrimer forward 27 CTTAAATCTTCAAATGCAGCAG Primer reverse 28F-CAAATGAAAACCCAGCTCACAAGAGTC-Q Probe forward 29F-TGGCATGCCATCCACACCAATTGA-Q Probe forward 30 ACTGGGCCATAAGGACCA Primerforward 31 CCGCTGAATGCTGCCATA Primer reverse 32F-AGTGGAGGAAATACCAATCAACAAAAGGC-Q Probe forward 33F-CGCTGCACTGAGAATGTAGGCTG-Q Probe reverse 34 GCGAACAATTCAACAGACAC Primerforward 35 GATTTCCCAGGATCCAGC Primer reverse 36F-TAGACACAGTACTAGAAAAGAATGTAACAG-Q Probe forward 37F-ATGCAATGGGGCTACCCCTCTTA-Q Probe reverse 38 ACGTGTTACCCAGGAGATTT Primerforward 39 CTTGGGGAATATCTCAAACC Primer reverse 40F-TCGATTATGAGGAGCTAAGAGAGCAAT-Q Probe forward 41F-ATTGCTCTCTTAGCTCCTCATAATCGA-Q Probe reverse 42 GTAACGGCAGCATGTCCTPrimer forward 43 TAGAGACTTTGTTGGTCAGC Primer reverse 44F-TGGTGAATGCCCCATAGCACGAG-Q Probe reverse 45 AGAATGAACTATTACTGGACACPrimer forward 46 GGACTGGTGTATCTGAAATG Primer reverse 47F-TAGAGCCGGGAGACAAAATAACATTC-Q Probe forward 48F-ACTGGAAATCTAGTGGTACCGAGATA-Q Probe forward 49F-TACCAGATCCAGCATTTCTTTCCATTG-Q Probe reverse 50 AGCACAAAATTGAGACTGGCPrimer forward 51 CCTGCTCATTTTGATGGTG Primer reverse 52F-CAGGATTGAGGAATGTCCCGTCTA-Q Probe forward 53F-ACCGTACCATCCATCTACCATCC-Q Probe reverse 54 ACAGTTCACAGCAGTAGGTA Primerforward 55 CTGGCTTCTTACCTTTTCATAT Primer reverse 56F-TTGATGATGGTTTCCTGGACATTTGGA-Q Probe forward 57F-TCTTCACATTTGAATCGTGGTAGTCCAAA-Q Probe reverse 58F-TCATTTTCCAATAGAACCAACAGTTCGG-Q Probe reverse 59GAAGCAAAATTAAACAGAGAAGAA Primer forward 60 TAGAGCACATCCAGAAACTGA Primerreverse 61 F-ATCAACAAGGATTTACCAGATTTTGGCGA-Q Probe forward 62F-ACCAATGAACTGGCGACAGTTGAATAGA-Q Probe reverse

The notations “F” and “Q” have been added to probe sequences in Table 1to indicate end-labeling the probe sequences with a fluorophore and aquencher, respectively. These notations are merely exemplary showing useof the probes for TaqMan PCR.

TABLE 2  Oligomer Sequences Targeting seasonal H1 Influenza A Virus SEQPreferred ID Sequence Function Direction 63 AGGTTTGTTTGGAGCCATTG Primerforward 64 TTGTTGAATTCTTTGCCCAC Primer reverse 65F-TCATTGAAGGGGGGTGGACTGG Probe forward AA-Q 66 F-TGGACTGGAATGGTAGATGGTTProbe forward GGT-Q 67 F-TCATTTTCTCAATTACAGAATT Probe reverseCACCTTGTTTG-Q 68 ATCATACAGAAAATGCTTATGT Primer forward 69MAGCAGAGTCCAGTAGTA Primer reverse 70 F-TTCACATTATAGCAGAAGATTC Probeforward ACCCCAG-Q 71 F-ACCCCAGAAATAGCCAAAAGAC Probe forward CC-Q 72TTGAGGCAAATGGAAATCTAATA Primer forward 73 TACATTCTGGAAAGGAAGACT Primerreverse 74 F-AGTAGAGGCTTTGGATCAGGAA Probe forward TCATC-Q 75F-TGTTTATAGCTCCCTGAGGTGT Probe reverse TTGACA-Q 76F-CATTGGTGCATTTGAGGTGATG Probe reverse ATTCCT-Q

The notations “F” and “Q” have been added to probe sequences in Table 2to indicate end-labeling the probe sequences with a fluorophore and aquencher, respectively. These notations are merely exemplary showing useof the probes for TaqMan PCR.

TABLE 3  Oligomer Sequences Targeting seasonal H3 Influenza A Virus SEQPreferred ID Sequence Function Direction 77 ACTAATGCTACTGAGCTGGT Primerforward 78 CTTATTTTGGAAGCCATCACA Primer reverse 79 F-ATCCTTGATGGAGAAAACTprobe forward GCACACTA-Q 80 F-AGGGTCTCCCAATAGAGCA probe reverseTCTATTAG-Q 81 F-TAGTGTGCAGTTTTCTCCA probe reverse TCAAGGAT-Q 82AAGACTATCATTGCTTTGAGCT Primer forward 83 TGAACCAGCTCAGTAGCATT Primerreverse 84 F-CTTCAATTTGGTCATTCGT probe reverse GATTGTTTTCAC-Q 85CTCTATTGGGAGACCCTCA Primer forward 86 CTTTCATTGTTAAACTCCAGTG Primerreverse 87 F-TGTGATGGCTTCCAAAATA probe forward AGAAATGGGA-Q 88TGCTCAAGCATCAGGAAGAAT Primer forward 89 CCCTAGGAGCAATTAGATTC Primerreverse 90 F-TCTACCAAAAGAAGCCAAC probe forward AAACTGTAAT-Q 91F-TGCTGTTAATCAAAAGTAT probe reverse GTCTCCCG-Q 92 AGCTCAATAATGAGATCAGATGPrimer forward 93 TTCCCTCCCAACCATTTTCT Primer reverse 94F-CCAAATGGAAGCATTCCCA probe forward ATGACAAAC-Q 95 F-CAAATATGCCTCTAGTTTGprobe reverse TTTCTCTGG-Q 96 TCTCAAAAGCACTCAAGCAG Primer forward 97CTCCGCGTTGTATGACCA Primer reverse 98 F-CAAATCAATGGGAAGCTGA probe forwardATAG(A/G)TTG-Q 99 CCTGGAGAACCAACATACAA Primer forward 100CAGGCATTGTCACATTTGTG Primer reverse 101 F-TGATCTAACTGACTCAGAA probeforward ATGAACAAACT-Q 102 F-ATCCTCAGCATTTTCCCTC probe reverse AGTTGCT-Q

The notations “F” and “Q” have been added to probe sequences in Table 3to indicate end-labeling the probe sequences with a fluorophore and aquencher, respectively. These notations are merely exemplary showing useof the probes for TaqMan PCR.

Although sequences are shown in Tables 1, 2, and 3 as DNA, RNA or mixedDNA/RNA sequences, the sequences are meant to include the correspondingDNA or RNA sequences, and their completely complementary DNA or RNAsequences. Particular embodiments of oligomers may include one or moremodified residues affecting the backbone structure (e.g., 2′-methoxysubstituted RNA groups), or one or more LNA monomers, preferably at 5′residues of a primer oligomer, or may include a non-nucleotide linker toattach a label to the oligomer. For example, oligomers that function asprobes for RNA targets may be synthesized with 2-methoxy substituted RNAgroups to promote more stable hybridization between probe and targetsequences. Embodiments include oligomers of the sequences abovesynthesized with 2′-methoxy substituted RNA groups and having anon-nucleotide linker (as described in U.S. Pat. No. 5,585,481) betweenresidues.

Particular embodiments of target capture oligomers include atarget-specific sequence that binds specifically to the swine H1N1influenza A virus, seasonal H1 Influenza A virus or seasonal H3Influenza A target nucleic acid and a covalently linked “tail” sequenceused in capturing the hybridization complex containing the targetnucleic acid to an immobilized sequence on a solid support. Particularembodiments of capture oligomers include at least one 2′ methoxylinkage. Embodiments of capture oligomers may include thetarget-specific sequence that binds to a swine H1N1 influenza A virus,seasonal H1 Influenza A virus or seasonal H3 Influenza A genomicsequence attached to another binding moiety, e.g., a biotinylatedsequence that binds specifically to immobilized avidin or streptavidin.The tail sequence or binding moiety binds to an immobilized probe (e.g.,complementary sequence or avidin) to capture the hybridized target andseparate it from other sample components by separating the solid supportfrom the mixture.

Primer sequences, including promoter primer sequences, bind specificallyto the target nucleic acid or its complementary sequence and may containadditional sequences that are not target-specific, e.g., the promotersequence in a promoter primer. A target-specific sequence, with orwithout an attached promoter sequence, may serve as an amplificationoligomer in a variety of in vitro amplification processes. Embodimentsof the swine H1N1 influenza A virus, seasonal H1 Influenza A virus orseasonal H3 Influenza A virus assays may use amplification methods thatrequire multiple cycling reaction temperatures, such as PCR (U.S. Pat.Nos. 4,683,195, 4,683,202, and 4,800,159), or may be substantiallyisothermal as in transcription associated amplification methods, such asTMA or NASBA (e.g., U.S. Pat. Nos. 5,399,491, 5,480,784, 5,824,518,5,888,779, 5,786,183, 5,437,990, 5,130,238, 4,868,105, and 5,124,246,and PCT Nos. WO 8801302 and WO 8810315). Particular embodiments of theswine H1N1 influenza A virus, seasonal H1 Influenza A virus or seasonalH3 Influenza A virus assays use PCR-based or TMA-based amplificationsystems that are detected during the amplification process (i.e., realtime detection) by including probes that emit distinguishablefluorescent signals when the probe is bound to the intended targetsequence made during the amplification process. Particular probes forreal time detection include those referred to as “TaqMan” (e.g., U.S.Pat. No. 5,691,146 Mayrand, U.S. Pat. No. 5,538,848 Livak), “molecularbeacon” or “molecular switch” probes (e.g., U.S. Pat. Nos. 5,118,801 and5,312,728, Lizardi et al., U.S. Pat. Nos. 5,925,517 and 6,150,097, Tyagiet al., Giesendorf et al., 1998, Clin. Chem. 44(3):482-6) and “moleculartorch” probes (e.g., U.S. Pat. Nos. 6,835,542 and 6,849,412, Becker etal.). Generally, such probes include a reporter dye attached to one endof the probe oligomer (e.g., FAM™, TET™, JOE™, VIC™) and a quenchercompound (e.g., TAMRA™, BLACK HOLE QUENCHERS™ or non-fluorescentquencher) attached to the other end of the probe oligomer, and signalproduction depends on whether the two ends with their attached compoundsare in close proximity or separated.

The assay to detect one or more of the specified influenza viruses in asample includes the steps of amplifying a target region in the targetinfluenza virus nucleic acid contained in a sample by usingamplification oligomers or primers specific for the intended targetregion, and then detecting the amplified nucleic acid. In some aspects,the detection step uses a detection probe oligomer with a targethybridizing sequence that is hybridized to the target nucleic acidand/or amplification products generated therefrom. Preferred assays usea PCR and detection is during the amplification reaction using adetection probe oligomer. For detection, the amplified nucleic acid maybe labeled and bound to an unlabeled probe, but particular embodimentsbind a labeled probe to the amplified nucleic acid. A particularembodiment for real-time detection uses a labeled probe that is detectedin a homogeneous system. In some aspects, the detection step isperformed using a technique such as gel electrophoresis, sequencing ormass spectrometry (e.g., U.S. Pat. Nos. 6,316,769, 6,011,496 and7,170,050 and US App. Pub. No. 2007/0087340).

Generally, the target influenza virus nucleic acid is separated fromother sample components before the amplification step. This may be doneby capturing the influenza virus nucleic acid by using a target-captureoligomer that binds to the target influenza virus nucleic acid, or byusing non-specific methods of purifying nucleic acid from a sample(e.g., U.S. Pat. Nos. 5,234,809, 5,705,628, 6,534,262 and 6,939,672, andInternational App. Pub. No. WO 2008/016988). Particular embodiments usea target-specific capture oligomer in a capturing step (U.S. Pat. Nos.6,110,678, 6,280,952 and 6,534,273). Embodiments of capture probesinclude those specific for swine H1N1 Influenza A virus, those specificfor the seasonal H1 Influenza A virus, and those specific for theseasonal H3 Influenza A virus. Preferably, the target capture probes arespecific for the subset of nucleic acids in a sample that are H1N1,seasonal H1 or seasonal H3. Embodiments of the probes specific for theseviruses include a dT₀₋₃dA₁₂₋₃₀ tail portion for hybridization to acomplementary immobilized probe sequence. Some embodiments of the probesinclude those wherein the nucleic acid tail portion is a left-handednucleic acid tail and hybridizes with an immobilized probe that is aleft-handed nucleic acid, while other embodiments use right-handed tailsand immobilized probes. Preferably, the influenza viral nucleic acidsare separated from other sample components by hybridizing the influenzanucleic acids to the target-hybridizing portion of the capture probe andhybridizing the tail portion of the capture probe to an immobilizedprobe that is attached to a solid support. This complex of captureprobe, its target influenza virus nucleic acid, and an immobilized probefacilitate separation of the influenza virus nucleic acid from othersample components, and optional washing steps may be used to furtherpurify the captured viral nucleic acid. Preferred solid supports includemagnetic particles, though other solid support work well, as is known inthe art. Alternatively, non-specific separation of viral RNA from othersample components is performed by adhering nucleic acids reversibly to asolid support, followed by washing and elution of the adhered nucleicacids into a substantially aqueous solution (e.g., using a MagNA Pure LCSystem (Roche) and the MagNA Pure Total Nucleic Acid Isolation Kit(Roche) or a NucliSENS easy MAG System (bioMériuex and the AutomatedMagnetic Extraction Reagents (bioMérieux) or comparable nucleic acidextraction instrument(s) and/or reagent kit(s)).

Amplifying the influenza virus target region using two primers may beaccomplished using a variety of known nucleic acid amplificationreactions, but preferably uses a PCR amplification (U.S. Pat. Nos.4,683,195, 4,683,202, and 4,800,159, Mullis et al.) to produce multipleDNA strands by using thermocycling reactions that separate dsDNA andprimers specific for portions of the separated strands to makeadditional dsDNA molecules by using a DNA polymerase. Well knownvariations of the basic PCR method may also be used, e.g.,reverse-transcriptase PCR that uses RT to produce a cDNA from an RNAtemplate, and then the DNA is amplified by PCR cycles, or PCR coupledwith real-time detection, both of which are sometimes referred to asRT-PCR.

Another embodiment of the influenza virus assay usestranscription-associated amplification reaction, such as TMA (describedin detail in U.S. Pat. Nos. 5,399,491 and 5,554,516). A TMA-based assayproduces many RNA transcripts (amplicons) from a single copy of targetnucleic acid or cDNA therefrom, and the amplicons are detected toindicate the presence of the target influenza virus in the sample.Briefly, in one example of a TMA-based assay, a promoter-primerhybridizes specifically to the target sequence and reverse transcriptase(RT) that includes RnaseH activity creates a first strand cDNA byextension from the 3′ end of the promoter-primer and digests thetemplate strand. The cDNA is then bound by a second primer and a newstrand of DNA is synthesized from the end of the second primer using RTto create a double-stranded DNA (dsDNA) containing a functional promotersequence. RNA polymerase specific for that promoter binds to thepromoter sequence and multiple RNA transcripts are produced, which eachcan act as a template for additional sequence replication using the samesteps used for the initial template. Thus, large amounts ofsingle-stranded amplified product are made using substantiallyisothermal reaction conditions.

Preferably, isolated influenza virus nucleic acid is then amplified forspecific target sequences contained the viral genome by using PCR or TMAamplification, and the amplification products are detected aftercompletion of the amplification reaction or during amplification (i.e.,real-time detection). For real-time detection, some embodiments may usea fluorophore-labeled probe (e.g., TaqMan, molecular beacon) that emitsa detectable signal only when the probe is hybridized to its targetsequence, and fluorescence is detected using standard fluorometry.Generally, assays detect at least two different probes (with different5′ fluorophores): an influenza virus-specific probe and an IC-specificprobe. Fluorescence is detected by using a system that incubates thereactions and detects fluorescence at different wavelengths at timeintervals during the reaction (e.g., DNA Engine OPTICON™ 2 system orCHROMO4™ Real-Time PCR Detector, Bio-Rad Laboratories, Inc., Hercules,Calif.). Real-time detected fluorescent signals in each channel areanalyzed using standard methods. For example, detected signals arenormalized to generate a best-fit curve to the data points for eachreaction (relative fluorescence vs. time) and results are reported asthe time of emergence when the signal met or exceeded a pre-set level.

Real-time reverse-transcriptase PCR-based assays (RT-PCR) are performedby using 50-500 nM solutions and 0.2 pmol/μl of probe in a 50 μlreaction that includes standard PCR reaction components. Incubation isperformed using: 48° C. for 30 min, 95° C. for 10 min, then 45 cycles of95° C. for 15 sec and cooling, and finally 60° C. for 1 min.Amplification and detection of the molecular beacon probe hybridized toits target amplified product are performed by using an open channelsystem (CHROMO4™, Bio-Rad Laboratories, Inc.) for real-time fluorescencedetection, with fluorescent signal readings taken at each of the 45cycles. Real-time fluorescence signals are analyzed and detection of theanalytes calculated from the fluorescence emergence curves by usingstandard methods.

The methods for detecting influenza virus nucleic acid include adetecting step that uses at least one probe that binds specifically tothe amplified influenza virus product (RNA or DNA amplicons).Preferably, the probe is labeled and produces a signal detected in ahomogeneous system, i.e., without separation of bound probe from unboundprobe. Particular probes are labeled with a fluorescent compound whichemits a detectable signal only when the probe is bound to its target,e.g., TaqMan, molecular switch, beacon, or torch probes. Otherparticular probes may be labeled with an acridinium ester (AE) compoundfrom which a chemiluminescent signal is produced and detected in ahomogeneous system (substantially as described in detail in U.S. Pat.Nos. 5,283,174, 5,656,744, and 5,658,737).

Particular embodiments of assays for detection of swine H1N1 Influenza Avirus, seasonal H1 Influenza A virus, and/or seasonal H3 Influenza Avirus nucleic acids include an internal control (IC) nucleic acid thatis amplified and detected by using IC-specific primers and probe in thesame reaction mixtures used for influenza virus nucleic acidamplification and detection (referred to herein as IC primers and ICprobe). Amplification and detection the IC-specific sequencedemonstrates that assay reagents and conditions are properly used evenwhen no influenza virus-specific signal is detected for a tested sample(i.e., negative samples). The IC may be used as an internal calibratorfor the assay that provides a quantitative result. A particular ICembodiment is a randomized sequence derived from a naturally occurringsource that is not an influenza virus (e.g., HIV).

Probes for detection of IC amplicons include any oligomer of at leastten residues that hybridizes specifically to a contiguous sequencecontained in the IC sequence or its complement (DNA or RNA) under assayconditions described herein. A particular IC-specific probe isexemplified by an oligomer labeled with a fluorescent compound at oneend and a quencher at the other end. In particular embodiments thatinclude an IC in an assay, the IC is treated throughout the assaysimilar to the intended analyte. For example, when a target capture stepis used for purification of the influenza virus nucleic acid target in asample, the target capture step includes a capture oligomer specific forthe IC to purify the IC from a mixture that includes the targetinfluenza virus nucleic acid and other sample components.

In general, methods used to demonstrate amplification and detection ofswine H1N1 influenza A virus, seasonal H1 Influenza virus A, or seasonalH3 Influenza Virus A nucleic acid by using the compositions describedherein in steps that include some sample preparation to isolate theinfluenza virus or its released nucleic acid from some other non-analytecomponents of the sample, followed by nucleic acid amplification of thetarget viral sequences, and detection of the amplified products toprovide information that identifies the amplified sequence(s) whichindicate the presence of the target influenza virus(es) in the sample.

Example 1 Extraction and Storage of Samples

Samples are taken from nasopharyngeal swabs (NPS) of patients presentingflu-like symptoms and the samples are each placed into approximately 3ml of viral transport medium (for example M4, M4RT, M5, or M6 media(Remel), UVT media (Becton Dickinson), or UTM media (Copan)). Sampleswere refrigerated for transport at 2-8° C., and stored at thattemperature for up to approximately 72 hours before processing. Sampleswhich needed longer storage were stored at ≦−70° C. Nucleic acids wereextracted from samples using standard laboratory methods to isolatenucleic acids (e.g., MagNA Pure LC System using the Total Nucleic AcidIsolation Kit (Roche) or the NucliSENS easyMAG System using theAutomated Magnetic Extraction Reagents (bioMérieux)). A positive controlsample is included which has a target sequence for each of the testedviral strains. That is, if the swine H1N1 influenza A virus is to betested, a swine H1N1 influenza A virus target sequence is included.Here, the positive controls were pooled RNA transcript from a portion ofan HA gene or of an NP gene for each of the subtypes of influenza. Inaddition, a negative control including the viral transport medium, butnot including a target sequence, and Internal Controls were extractedalongside the samples.

Example 2 The Uniplex Reactions

Once the primers are chosen, as described above, the primers are testedagainst its target in a PCR amplification assay.

Materials: PCR Master Mix containing about 2 mM MgCl₂ and about 0.8 mMdNTPs when diluted to 1× (Roche); Taq DNA Polymerase (Roche); RNAseInhibitor 40 u/μL; Reverse Transcriptase 10 u/μL; InfluenzaA/Jianxi/160/05(H1N1) 1×10^(5.5) TCID₅₀/ml (seasonal H1 Influenza Avirus strain); Influenza A/Hong Kong/218/08 (H3N2) 1×10^(5.25) TCID₅₀/ml(seasonal H3 Influenza A virus strain); Influenza A H1N1-Swine FluClinical specimen (swine H1N1 influenza A virus strain); an Internal RNAControl nucleic acid; and Remel M4-Viral Transport Medium (VTM). Formost uniplex reactions, primers were used at approximately 50 μM andprobes at approximately 10 μM.

Procedure: Extraction and dilution of samples was completed on theeasyMAG and 0.200 ml input and 55 μL elution volumes using the genericprotocol 2.0.1 (available from bioMérieux). 63.2 μL of InfluenzaA/Jiangxi/160/05 (H1N1)+136.8 μL VTM=200 μL of 1×10⁵ TCID₅₀/ml; and 84.4μL of Influenza A/Hong Kong/218/06 (H3N2) 1×10^(5.25) TCID₅₀/ml+65.6VTM=150 μL of 1×10⁵ TCID₅₀/ml. 180 μL VTM is added to 12 sample vesselwells and 20 μL of each of the above dilutions were added to 6 of thewells. 200 μL of H1N1 Swine clinical specimen was added to 6 wells. 180μL of VTM was added to the final 6 wells and 20 μL of previouslyprepared RNA Internal Control (IC) was added to each of the wells. Eachof the 6 extractions per subtype is mixed and then aliquoted into 6×50μL samples for use, and then stored at −≦70° C.

Mixing the Primers and Probes: The primers and probes designed asdescribed above are synthesized by means known to those of skill in theart. The primers and probes are mixed prior to the testing. For example,when testing the primers and probes targeting the NP gene of swine H1N1influenza A virus from Table 1, (SEQ ID NOS:1, 2, 5, 6, 8, 9, 12, 13,17, 18, 21, 22, 26, 27, 30 or 31 for primers and SEQ ID NOS:3, 4, 7, 10,11, 14-16, 19, 20, 23-25, 28, 29, 32 or 33 for probes) the followingmixes are made. The same is done for the primers and probes of Tables1-3 that target the HA gene of the swine H1N1 influenza A virus,seasonal H1 influenza A virus and seasonal H3 influenza A virus.

MiniMix: 2x PCR Master Mix 12.5 μL Forward Primer  0.100 Reverse Primer 0.100 Water  5.25 Total 17.95

Supermix: Minimix 17.95 μL Probe  0.500 Reverse Transcriptase  0.300RNase Inhibitor  0.25 Taq 5 u/μL  1 Total 20

Under this general protocol, the various probes can be labeled with anyof the fluorescent labels. However, in the present example, the probestargeting seasonal H1 Influenza A virus were detected in the FAM channel(520 nm peak), probes targeting seasonal H3 Influenza A virus in the TETchannel (561 nm peak), probes targeting the swine H1N1 influenza A virusin the TX Red channel (651 nm peak), and the internal control in the Cy5channel (667 nm peak). In the present instance, the SEQ ID NO:3 probewas not detected in the FAM, CY5 or TET channels, but was detected inthe TX Red channel. Detection probe oligomers can be labeled with avariety of different fluorescent labels, and are not limited to theseshown in the examples. Combinations of primers and probes for a swine NPuniplex reaction included, SEQ ID NOS; 1 & 2 with 3 and/or 4; 5-7; 8 & 9with 10 and/or 11; 12 & 13 with 14, 15 and/or 16; 17 & 18 with 19 and/or20; 21 & 22 with 23, 24 and/or 25; 26 & 27 with 28 and/or 29; and 30 &31 with 32 and/or 33. The protocol for thermocycling is as follows: 42°C. for 30 min, 95° C. for 10 min, 5 cycles of 95° C. for 30 sec, 55° C.for 1 min, 45 cycles of 95° C. for 1 min (detection at this step).

Using a primer probe combination of SEQ ID NOS:1-3, the followingresults were obtained:

TABLE 4 Sample TX Red (Ct) Seasonal H1 Influenza A 28.9  Seasonal H3Influenza A — Swine H1N1 Influenza A 16.36 Negative Control — water —

Here, SEQ ID NOS:1-3 detected Swine H1N1 Influenza A virus, however,there was also some cross reactivity with the seasonal H1 Influenza Avirus. Therefore, SEQ ID NOS:1-3 are useful for generally detecting thepresence of influenza A viruses. However, if the objective is toselectively detect and differentiate influenza types, this combinationwould show cross reactivity with seasonal influenza A viruses, makingdata interpretation difficult.

In contrast, other primer and probe sets were more specific. Table 5includes results for SEQ ID NOS:1, 2 & 4; 1, 2 & 7; 3, 5 & 6; 5, 6 & 7;8, 9 & 10; and 8, 9 & 11, indicating specificity by means of the TX Redvalues.

TABLE 5 Primer/Probe Sample TX Red (Ct) SEQ ID NOS: 1, 2 & 4 Seasonal H1Influenza A — Seasonal H3 Influenza A — Swine H1N1 Influenza A 17.67Negative Control — water — SEQ ID NOS: 1, 2 & 7 Seasonal H1 Influenza A— Seasonal H3 Influenza A — Swine H1N1 Influenza A 17.88 NegativeControl — water — SEQ ID NOS: 3, 5 & 6 Seasonal H1 Influenza A 27.78Seasonal H3 Influenza A — Swine H1N1 Influenza A 17.52 Negative Control— water — SEQ ID NOS: 5-7 Seasonal H1 Influenza A — Seasonal H3Influenza A — Swine H1N1 Influenza A 18.55 Negative Control — water —SEQ ID NOS: 8-10 Seasonal H1 Influenza A — Seasonal H3 Influenza A 33.09Swine H1N1 Influenza A 19.13 Negative Control — water — SEQ ID NOS: 8, 9& 11 Seasonal H1 Influenza A — Seasonal H3 Influenza A — Swine H1N1Influenza A 19.02 Negative Control — water —

Similar uniplex tests were conducted for each of the primer and probesets described above in Tables 1-3.

Example 3 Reactivity and Specificity of the PCR-Based Swine H1N1Influenza A Virus Singleplex Assay, the Seasonal H1 Influenza A VirusSingleplex Assay, or the Seasonal H3 Influenza A Virus Singleplex Assaywith the Seasonal H1 Influenza A Virus and the Seasonal H3 Influenza AVirus

This example demonstrates the reactivity and specificity of thePCR-based swine H1N1 influenza A singleplex assay, the seasonal H1Influenza A singleplex assay, or the seasonal H3 Influenza A singleplexassay, with the seasonal H1 Influenza A virus and the seasonal H3Influenza A virus, which specifically detected the intended viral targetfor each test. The PCR-based swine H1N1 influenza A virus assay,seasonal H1 Influenza A virus assay, and the seasonal H3 Influenza Avirus assay were performed substantially as described in Example 2.

An IC RNA was included in all of the tests to demonstrate that the assayconditions and amplification and detection steps were performedappropriately to detect the IC target (or any cross-reactive target) inthe sample.

Each sample containing a known virus was tested independently using thePCR-based swine H1N1 influenza A virus, seasonal H1 Influenza A virus orthe seasonal H3 Influenza A virus test with the same IC. Separate swineH1N1 influenza A virus, seasonal H1 Influenza A virus, and seasonal H3Influenza A virus nucleic acid assays were performed simultaneouslyunder the same conditions using positive control samples that containedthe relevant virus targets.

Positive controls included fourteen sources of H1N1 influenza A virus(which may or may not be a swine H1N1 influenza A virus as denotedbelow) and 15 sources of seasonal H3 Influenza A virus, each testedindividually at 10⁵ and 10² copies per reaction (samples were obtainedfrom American Type Culture Collection (ATCC) accession numbers providedbelow, CDC, or the University of Wisconsin, and were grown and titeredby Tricore Reference Laboratories). Positive control samples for H1N1Influenza A virus included:

VR 1620 A/WS/33 5×10^(5.75) TCID₅₀/ml; at use 5×10^(3.75)

A/Virginia/1/08 1×10⁴ TCID₅₀/ml; at use 1×10²

A/Fuijan/158/00 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Taiwan/42/06 1×10^(3.5) TCID₅₀/ml; at use 1×10¹⁵

VR 997 A/New Jersey/8/76 5×10^(6.25) TCID₅₀/ml; at use 5×10^(4.25)

Brazil/1137/99 6.8×10⁶ TCID₅₀/ml; at use 6.8×10⁴

A/Kentucky/2/06 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Henan/8/05 1×10^(4.5)TCID₅₀/ml; at use 1×10^(2.5)

VR 98 A1/Mal/302/54 5×10^(7.25) TCID₅₀/ml; at use 5×10^(5.25)

VR 546 A1/Denver/1/57 5×10^(7.25)TCID₅₀/ml; at use 5×10^(5.25)

A/Hong Kong/2506/06 1×10⁴ TCID₅₀/ml; at use 1×10²

A/PR/9/34 1×10⁸ TCID₅₀/ml; at use 1×10⁶

A/Hawaii/15/01 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/New Caledonia/12/99 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

Positive control samples for the H3N2 Influenza A virus included:

VR 822 A/Victoria/3/75 5×10^(7.25) TCID₅₀/ml; at use 5×10^(5.25)

VR 547 A/Aichi/2/69 5×10^(5.5) TCID₅₀/ml; at use 5×10^(3.5)

A/Brazil/02/99 1.9×10⁶ TCID₅₀/ml; at use 1.9×10⁴

A/New York/55/2004 1×10⁵ TCID₅₀/ml; at use 1×10³

A/Hong Kong/2831/05 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Port Chalmers/1/73 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Hahmas/2696/99 9.3×10⁷ TCID₅₀/ml; at use 9.3×10⁵

VR 544 A/Hong Kong/6/68 5×10^(5.75) TCID₅₀/ml; at use 5×10^(3.75)

A/California/07/04 1×10^(4.5) TCID₅₀/ml; at use 5×10^(2.5)

A/Hiroshima/53/05 1×10⁵ TCID₅₀/ml; at use 1×10³

A/Fuijan/411/02 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Kentucky/03/06 1×10^(5.5) TCID₅₀/ml; at use 1×10^(3.5)

A/Costa Rica/07/99 2×10⁷TCID₅₀/ml; at use 2×10⁵

A/Anhui/1239/05 1×10^(4.5) TCID₅₀/ml; at use 1×10^(2.5)

A/Victoria/512/05 1×10⁵ TCID₅₀/ml; at use 1×10³

Note, strain VR 897 A/New Jersey/8/76 (HSW N1) is a recombinant H1N1human and swine influenza A virus.

In addition, the primers and probes were tested against nucleic acidsextracted from clinical samples from patients identified to have the2009 H1N1 Influenza A virus.

Supermixes are generated for each of the primers and probes as describedin Example 2. The concentrations of the primers and probes in the mixesmay range from 50-500 nM. For instance, various primers or probesperform best at 50 nM, 75 nM, 100 nM, 150 nM, 200 nM, 250 nM, 300 nM,350 nM, 400 nM, 450 nM, or 500 nM.

The PCR-based swine H1N1 influenza A virus, seasonal H1 influenza Avirus assay, and seasonal H3 influenza A virus assays are performed byusing primers and probes as described in Table 1-3 for real-timedetection of the PCR amplicons. The reactions included an IC that isamplified and detected by using primers/probes specific to the internalcontrol. Internal control sequences are known in the art. Additionalpositive controls are tested at the same time using the same conditionsbut using samples that contained known amounts of an H1N1 influenza Avirus or H3N2 influenza A virus target.

The PCR-based seasonal H1 influenza A virus assay gave positive resultsfor all tested samples that contained H1N1 influenza virus A nucleicacids and negative results for most of the control samples thatcontained H3N2 virus samples. Similarly, the PCR-based seasonal H3influenza A virus assay gave positive results for all tested samplesthat contained H3N2 influenza A nucleic acids and negative results forall H1N1 influenza A control samples.

Sequences are eliminated from further study for various reasonsincluding failure to react with their intended target (e.g., SEQ IDNO:10 and SEQ ID NO:32 probes do not react consistently well with the2009 H1N1 influenza A strain target nucleic acids), and, becauseselective detection of H1N1, seasonal H1 or seasonal H3 was desired forthis example, for cross reactivity to an unintended target nucleic acid(e.g., SEQ ID NO:40, SEQ ID NO: 41, and SEQ ID NO:49 react with theA/Kentucky/2/06 H1N1 strain). Other reasons to eliminate sequences werebased on combinations of probes and primers which led to non-specificinteractions, primer dimer formation, disparate primer amplificationefficiencies or overall poor amplification, such with SEQ ID NO:53.

During the singleplex testing, 2 of the 27 mixes using primers andprobes specific for the swine H1N1 influenza A virus did not react tothe swine H1N1 influenza A virus test sample. Of the 25 primer/probesets specific for the swine H1N1 influenza A virus, 2 of them reactedbut had nonspecific amplification. 3 of the 11 primer/probe sets whichtargeted seasonal H3 Influenza A did not react and additional 1 of the11 was eliminated for having an extremely late Ct.

Thus, 23 and 7 combinations of primers and probes specific for the swineH1N1 influenza A virus and seasonal H3 influenza A virus were found tobe useful in a singleplex assay. Results from an Agilent BioAnalyzer gelshowed that the H3N2 strain A/Kentucky/03/06 (#24) amplified with SEQ IDNOS:12 & 13 with 15 or 16 primers/probes at the correct size. The gelalso showed that the seasonal H3 influenza A strain VR 822A/Victoria/3/75 (#15) amplifies with the SEQ ID NOS:21 & 22 with 23, 24or 25 primers/probe at the correct size. Strains VR 547 A/Aichi/2/69(#16) and A/Costa Rica/07/99 (#22) amplify as well, but in triplicate,and not at the correct size, even though there is real timeamplification.

The mixes of primers and probes were then optimized in the singleplexassay, by methods known to those of skill in the art, for example, byoptimizing the concentration of the primer and/or probe in the mixture,by optimizing the amount of dNTPs used, through the addition of BSA oradditional MgCl₂, or the amount of Taq Enzyme used.

Example 4 Detection of Swine H1N1 Influenza A Virus in a MultiplexReaction with Seasonal H1 Influenza A Virus and Optionally Seasonal H3Influenza A Virus

This example describes tests to determine whether the primers and probesselected from the singleplex tests above for specificity and selectivitywere as effective if used in a multiplex reaction with primers, probes,and reagents for seasonal H1 Influenza A and possibly seasonal H3Influenza A.

PCR-based swine H1N1 assays were performed substantially as described inExample 2, using primers sets from Tables 1-3 to amplify target RNAtranscripts and detecting the amplicons by using a fluorophore-labeledprobes from Tables 1-3. However, mixes of primers and probes specificfor the nucleotide sequence encoding swine H1N1 influenza A virus NPgene or swine H1N1 influenza A HA gene were combined with primers andprobes specific for seasonal H1 Influenza A virus and optionally theseasonal H3 Influenza A virus.

Various primer/probe combinations are eliminated based on this multiplextesting. For instance, when SEQ ID NO:45, SEQ ID NO:46, and SEQ ID NO:48were tested in combination with SEQ ID NO:72, SEQ ID NO:73 and SEQ IDNO:74 (quencher in the middle of the probe), and SEQ ID NO:99, SEQ IDNO:100, and SEQ ID NO:102, and the Internal Control, there was a nonspecific amplification channel with water, poor sensitivity for seasonalH3 Influenza A virus strains (detected 1/3 dilutions), poor sensitivityfor the seasonal H1 Influenza A virus strains (detected 1/3) and poorsensitivity for the swine H1N1 influenza A virus strains (detected 1/3).Similar sensitivity issues were found for the SEQ ID NO:50, SEQ IDNO:51, and SEQ ID NO:52 probe/primer set. Likewise, with primers andprobes designed to be specific for the seasonal H3 Influenza A virus,certain probes when used in combination with specific primers and probestargeting seasonal H1 influenza A virus nucleic acids or specificprimers and probes targeting swine H1N1 influenza A virus nucleic acidswere not sufficiently sensitive, or selective enough for them to providea robust signal in the multiplex format, for example, SEQ ID NOS: 94, 98and 102. These combinations of primer/probe sets are subsequentlyeliminated from further study.

Once the primers and probes are initially tested in the multiplexformat, the positive samples are titrated down to identify primers andprobes for detecting lowered doses of each of the virus types.

Example 5 Detection of Influenza Virus in Clinical Samples

This example describes primer and probe combinations for use in amultiplex real-time RT-PCR assay to detect and differentiate betweenseasonal H1 Influenza A virus, seasonal H3 Influenza A virus, and swineH1N1 Influenza A virus. The assay detects the amplicons in real time andprovides positive results for samples that contain the target influenzavirus. Assays are performed substantially as described in Example 3, butusing an aliquot of prepared clinical sample nucleic acid in place ofthe target influenza virus RNA transcripts.

Samples are taken from patients and stored in accordance with Examples 1and 2. Assays are performed substantially as described in Example 3using an aliquot of prepared clinical sample nucleic acid. Fluorescentlabels are detected and Ct value indicated that a sample contained agiven target nucleic acid.

Before any assays that evaluate the sensitivity and selectivity of theprimer/probe combinations are performed, the samples are first testedusing the CDC rRT-PCR Flu Panel (IVD) to detect seasonal influenza A/H1and A/H3 or the CDC rRT-PCR Swine Flu Panel (EUA) to detect 2009 H1N1influenza A virus. Each sample containing a known virus is testedindependently using the PCR-based swine H1N1 influenza A virus, seasonalH1 Influenza A virus or the seasonal H3 Influenza A virus test with thesame IC. Separate swine H1N1 influenza A virus, seasonal H1 Influenza Avirus, and seasonal H3 Influenza A virus nucleic acid assays areperformed simultaneously under the same conditions using positivecontrol samples that contained the relevant virus targets. Exemplarymultiplex mixes are described below (each also including primers and aprobe to an internal control).

Primer/ Name Probe Mixture 1: SEQ ID NO: 72 Primer SEQ ID NO: 73 PrimerSEQ ID NO: 74 Probe SEQ ID NO: 77 Primer SEQ ID NO: 78 Primer SEQ ID NO:79 Probe SEQ ID NO: 1 Primer SEQ ID NO: 2 Primer SEQ ID NO: 4 ProbeMixture 2: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 ProbeSEQ ID NO: 99 Primer SEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ IDNO: 42 Primer SEQ ID NO: 43 Primer SEQ ID NO: 44 Probe Mixture 3: SEQ IDNO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 99Primer SEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 26 PrimerSEQ ID NO: 27 Primer SEQ ID NO: 29 Probe Mixture 4: SEQ ID NO: 72 PrimerSEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 Primer SEQ ID NO:100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 54 Primer SEQ ID NO: 55Primer SEQ ID NO: 57 Probe Mixture 5: SEQ ID NO: 72 Primer SEQ ID NO: 73Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 Primer SEQ ID NO: 100 PrimerSEQ ID NO: 102 Probe SEQ ID NO: 1 Primer SEQ ID NO: 2 Primer SEQ ID NO:4 Probe Mixture 6: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO:74 Probe SEQ ID NO: 92 Primer SEQ ID NO: 93 Primer SEQ ID NO: 94 ProbeSEQ ID NO: 17 Primer SEQ ID NO: 18 Primer SEQ ID NO: 20 Probe Mixture 7:SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO:92 Primer SEQ ID NO: 93 Primer SEQ ID NO: 94 Probe SEQ ID NO: 12 PrimerSEQ ID NO: 13 Primer SEQ ID NO: 15 Probe Mixture 8: SEQ ID NO: 72 PrimerSEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 92 Primer SEQ ID NO:93 Primer SEQ ID NO: 94 Probe SEQ ID NO: 12 Primer SEQ ID NO: 13 PrimerSEQ ID NO: 16 Probe Mixture 9: SEQ ID NO: 72 Primer SEQ ID NO: 73 PrimerSEQ ID NO: 74 Probe SEQ ID NO: 92 Primer SEQ ID NO: 93 Primer SEQ ID NO:94 Probe SEQ ID NO: 21 Primer SEQ ID NO: 22 Primer SEQ ID NO: 23 ProbeMixture 10: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74Probe SEQ ID NO: 92 Primer SEQ ID NO: 93 Primer SEQ ID NO: 94 Probe SEQID NO: 21 Primer SEQ ID NO: 22 Primer SEQ ID NO: 25 Probe Mixture 11:SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO:96 Primer SEQ ID NO: 97 Primer SEQ ID NO: 98 Probe SEQ ID NO: 17 PrimerSEQ ID NO: 18 Primer SEQ ID NO: 20 Probe Mixture 12: SEQ ID NO: 72Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 96 Primer SEQID NO: 97 Primer SEQ ID NO: 98 Probe SEQ ID NO: 12 Primer SEQ ID NO: 13Primer SEQ ID NO: 15 Probe Mixture 13: SEQ ID NO: 72 Primer SEQ ID NO:73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 96 Primer SEQ ID NO: 97 PrimerSEQ ID NO: 98 Probe SEQ ID NO: 12 Primer SEQ ID NO: 13 Primer SEQ ID NO:16 Probe Mixture 14: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ IDNO: 74 Probe SEQ ID NO: 96 Primer SEQ ID NO: 97 Primer SEQ ID NO: 98Probe SEQ ID NO: 21 Primer SEQ ID NO: 22 Primer SEQ ID NO: 23 ProbeMixture 15: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74Probe SEQ ID NO: 96 Primer SEQ ID NO: 97 Primer SEQ ID NO: 98 Probe SEQID NO: 21 Primer SEQ ID NO: 22 Primer SEQ ID NO: 25 Probe Mixture 16:SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO:99 Primer SEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 17Primer SEQ ID NO: 18 Primer SEQ ID NO: 20 Probe Mixture 17: SEQ ID NO:72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 PrimerSEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 12 Primer SEQ IDNO: 13 Primer SEQ ID NO: 15 Probe Mixture 18: SEQ ID NO: 72 Primer SEQID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 Primer SEQ ID NO: 100Primer SEQ ID NO: 102 Probe SEQ ID NO: 12 Primer SEQ ID NO: 13 PrimerSEQ ID NO: 16 Probe Mixture 19: SEQ ID NO: 72 Primer SEQ ID NO: 73Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 Primer SEQ ID NO: 100 PrimerSEQ ID NO: 102 Probe SEQ ID NO: 21 Primer SEQ ID NO: 22 Primer SEQ IDNO: 23 Probe Mixture 20: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQID NO: 74 Probe SEQ ID NO: 99 Primer SEQ ID NO: 100 Primer SEQ ID NO:102 Probe SEQ ID NO: 21 Primer SEQ ID NO: 22 Primer SEQ ID NO: 25 ProbeMixture 21: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74Probe SEQ ID NO: 99 Primer SEQ ID NO: 100 Primer SEQ ID NO: 102 ProbeSEQ ID NO: 26 Primer SEQ ID NO: 27 Primer SEQ ID NO: 28 Probe Mixture22: SEQ ID NO: 72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ IDNO: 99 Primer SEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 42Primer SEQ ID NO: 43 Primer SEQ ID NO: 44 Probe Mixture 23: SEQ ID NO:72 Primer SEQ ID NO: 73 Primer SEQ ID NO: 74 Probe SEQ ID NO: 99 PrimerSEQ ID NO: 100 Primer SEQ ID NO: 102 Probe SEQ ID NO: 54 Primer SEQ IDNO: 55 Primer SEQ ID NO: 57 Probe

Results are obtained by measuring the Ct and/or RFU corresponding toeach of the fluorescent signals as described above for each targetstrain.

Exemplary results: For mixture 1 the following results are obtained forthe various target strains. Of the 168 samples tested, 24 samples areknown to be positive for seasonal H1 Influenza A virus, the multiplexassay detected 23 of these samples. Of the 168 samples tested, 20 areknown to be positive for the Seasonal H3 Influenza A virus, and all 20are detected. Likewise, 52 of the 168 samples are known to be positivefor swine H1N1 Influenza A. The assay detects 50 of those samples.

The invention being thus described, it will be apparent to one ofordinary skill in the art that various modifications of the materialsand methods for practicing the invention can be made. Such modificationsare to be considered within the scope of the invention as defined by thefollowing claims.

Each of the references from the patent and periodical literature citedherein is hereby expressly incorporated in its entirety by suchcitation.

We claim:
 1. A composition comprising: a pair of H1N1 influenza-specificamplification primers, wherein the primers comprise: (a) (i) a firstnucleic acid oligonucleotide primer having at least 18 contiguousnucleotides encoding the influenza A NP protein, specific for swine H1N1influenza A virus, or their completely complementary sequences, or DNAequivalents thereof; and (ii) a second nucleic acid oligonucleotideprimer having at least 18 contiguous nucleotides encoding the influenzaA NP protein, specific for swine H1N1 influenza A virus, or theircompletely complementary sequences, or DNA equivalents thereof; and/or(b) (i) a first nucleic acid oligonucleotide primer having at least 18contiguous nucleotides encoding the H1 influenza A protein, specific forswine H1N1 influenza A virus, or their completely complementarysequences, or DNA equivalents thereof; and (ii) a second nucleic acidoligonucleotide primer having at least 18 contiguous nucleotidesencoding the H1 influenza A protein, specific for H1N1 influenza Avirus, or their completely complementary sequences, or DNA equivalentsthereof.
 2. The composition according to claim 1, that further comprisesa first swine H1N1 influenza A virus-specific oligonucleotide detectionprobe having at least 18 contiguous nucleotides of the sequence encodingeither the H1 protein or the NP protein of the swine H1N1 influenza Avirus.
 3. The composition according to claim 1 or 2, wherein each ofsaid oligonucleotides includes one or more nucleic acids at the 5′ endthat do not correspond to a portion of said influenza protein, andwherein said nucleic acid primer and said probe are no more than 50nucleic acids in length.
 4. The composition according to claim 2,wherein said detection probe comprises at least a first detectable labeloperably linked to said oligonucleotide detection probe.
 5. Thecomposition of claim 2, wherein at least one of the labels is located atthe 5′ end of an oligonucleotide, is bound to the oligonucleotidethrough a nucleic acid which is not the 5′ or 3′ terminal nucleic acid,or is intercalating.
 6. The composition according to any one of claims3-5, wherein the label is detectable in a homogeneous assay system. 7.The composition according to claim 2, wherein said primers are SEQ IDNO:1 and SEQ ID NO:2 and said probe is SEQ ID NO:4.
 8. The compositionaccording to claim 2, wherein said primers are SEQ ID NO:72 and SEQ IDNO:43 and said probe is SEQ ID NO:44.
 9. The composition of any one ofclaims 1-8, wherein said first and second nucleic acid oligonucleotideprimers are in the form of a kit.
 10. A kit comprising, in a suitablecontainer, said pair of H1N1 influenza A virus-specific amplificationprimers according to any one of claims 1-8, and instructions for use ofsaid first pair of primers in a PCR amplification of polynucleotides ina biological sample.
 11. A kit comprising, in a suitable container, saidoligonucleotide primers and said oligonucleotide detection probeaccording to any one of claims 2-8, and instructions for use of saidfirst pair of primers in a PCR amplification of polynucleotides in abiological sample suspected to contain a swine H1N1 influenza A virusnucleic acid segment or fragment.
 12. A composition comprising at leasttwo seasonal H1 influenza A-specific amplification primers, wherein theprimers comprise a nucleic acid oligonucleotide primer having at least18 contiguous nucleotides encoding the H1 protein of H1 influenza A, ortheir completely complementary sequences, or DNA equivalents thereof.13. The composition according to claim 12, that further comprises aseasonal H1 influenza A-specific oligonucleotide detection probe havingat least 18 contiguous nucleotides of the sequence encoding the H1protein of the seasonal H1 influenza A.
 14. The composition according toany one of claim 12 or 13, wherein each of said oligonucleotidesincludes one or more nucleic acids at the 5′ end that do not correspondto a portion of said influenza protein, and wherein said nucleic acidprimer and said probe are no more than 50 nucleic acids in length. 15.The composition according to claim 13, wherein said detection probecomprises at least a first detectable label operably linked to saidoligonucleotide detection probe.
 16. The composition according to claim13, wherein said primers are SEQ ID NO:72 and SEQ ID NO:73 and saidprobe is SEQ ID. NO.
 74. 17. A composition comprising at least twoseasonal H3 influenza A-specific amplification primers, wherein theprimers comprise a nucleic acid oligonucleotide primer having at least18 contiguous nucleotides encoding the H3 protein from seasonal H3influenza A, or their completely complementary sequences, or DNAequivalents thereof.
 18. The composition according to claim 17, thatfurther comprises a seasonal H3 seasonal influenza A-specificoligonucleotide detection probe having at least 18 contiguousnucleotides of the sequence encoding the H3 protein of the H3 seasonalinfluenza A.
 19. The composition according to any one of claim 17 or 18,wherein each of said oligonucleotides has one or more additional nucleicacids at the 5′ end do not correspond to a portion of said influenzaprotein, and wherein said nucleic acid primer and said probe are no morethan 50 nucleic acids in length.
 20. The composition according to claim19, wherein said detection probe comprises at least a first detectablelabel operably linked to said oligonucleotide detection probe.
 21. Thecomposition according to claim 18, wherein said primers are SEQ ID NO:99and SEQ ID. NO. 100 and said probe is SEQ ID NO:102.
 22. A kitcomprising the compositions according to claims 7, 16 and
 21. 23. A kitcomprising the compositions according to claims 8, 16 and
 21. 24. Amethod for detecting the presence or absence of an H1N1 influenza Avirus nucleic acid segment in a population of polynucleotides in asample, which method comprises: (a) contacting the sample with acomposition according to any one of claims 1-8 to produce a swine H1N1influenza amplification product if a swine H1N1 influenza A virusnucleic acid segment is present in said sample; (b) contacting saidamplification product with a swine H1N1 influenza A virus-specificoligonucleotide specific detection probe according to claim 4; and (c)detecting the presence of said amplification product, wherein thepresence of said amplification product is indicative of the presence ofone or more swine H1N1 influenza A virus-specific nucleic acid segmentsin said population of polynucleotides.
 25. A method for detecting thepresence or absence of an H1N1 influenza A virus nucleic acid segment ina population of polynucleotides in a sample, which method comprises: (a)contacting the sample with the primers in the composition according toclaim 7 or 8 to produce a swine H1N1 influenza A virus amplificationproduct if a swine H1N1 influenza nucleic acid segment is present insaid sample; (b) contacting said amplification product with a swine H1N1influenza A virus-specific oligonucleotide specific detection probe inthe composition according to claim 7 or 8; and (c) detecting thepresence of said amplification product, wherein the presence of saidamplification product is indicative of the presence of one or more swineH1N1 influenza A virus-specific nucleic acid segments in said populationof polynucleotides.
 26. A composition for detecting the presence ofswine H1N1 influenza virus comprising at least two oligonucleotidesspecific for sequences in that represent a H1N1 influenza virus genomeor transcripts made from the H1N1 influenza virus genome, selected fromthe group consisting of: SEQ ID NO: 1 AAGTCGAAACCCAGGAAAC SEQ ID NO: 2CATGCCCACTTGCTACTG SEQ ID NO: 3 CATACACACAAGCAGGCAGGCA SEQ ID NO: 4AAGACCTCATTTTCCTGGCACGGT SEQ ID NO: 5 CACGGTCAGCACTCATTC SEQ ID NO: 6TTCAAAGTCATGCCCACTTG SEQ ID NO: 7 ATCAGTTGCACATAAATCCTGCCTG SEQ ID NO: 8ATTGGTGGAATCGGGAGATT SEQ ID NO: 9 AGGTATTTATTTCTTCTCTCATC SEQ ID NO: 10TCCAAATGTGCACTGAACTCAAACTC SEQ ID NO: 11 TAGTCGTCCATCATAATCACTGAGTTTSEQ ID NO: 12 TGGCGTCTCAAGGCACC SEQ ID NO: 13 TTCCACCAATCATTCTTCCGASEQ ID NO: 14 ATCATATGAACAAATGGAGACTGGTGG SEQ ID NO: 15CGCCAGGATGCCACAGAAATCAGA SEQ ID NO: 16 TGCTCTGATTTCTGTGGCATCCTGGSEQ ID NO: 17 TAGAAGAGCATCCCAGTGC SEQ ID NO: 18 CCATTGTTTGCTTGGCGCSEQ ID NO: 19 AAGGACCCTAAGAAAACAGGAGGACC SEQ ID NO: 20TTCTTCTTTGTCATAAAGGATGAGTTCTC SEQ ID NO: 21 CAACCTGAATGATGCCACATSEQ ID NO: 22 TCGGTCATTGATTCCACGTT SEQ ID NO: 23 AGAGCGCTTGTTCGCACCGGAATSEQ ID NO: 24 CAGAATGTGCTCTCTAATGCAAGGTTC SEQ ID NO: 25TCATTCTGATTAACTCCATTGCTATTGTTCC SEQ ID NO: 26 AGTGGTCAGCCTGATGAGASEQ ID NO: 27 CTTAAATCTTCAAATGCAGCAG SEQ ID NO: 28CAAATGAAAACCCAGCTCACAAGAGTC SEQ ID NO: 29 TGGCATGCCATCCACACCAATTGASEQ ID NO: 30 ACTGGGCCATAAGGACCA SEQ ID NO: 31 CCGCTGAATGCTGCCATASEQ ID NO: 32 AGTGGAGGAAATACCAATCAACAAAAGGC SEQ ID NO: 33CGCTGCACTGAGAATGTAGGCTG SEQ ID NO: 34 GCGAACAATTCAACAGACAC SEQ ID NO: 35GATTTCCCAGGATCCAGC SEQ ID NO: 36 TAGACACAGTACTAGAAAAGAATGTAACAGSEQ ID NO: 37 ATGCAATGGGGCTACCCCTCTTA SEQ ID NO: 38 ACGTGTTACCCAGGAGATTTSEQ ID NO: 39 CTTGGGGAATATCTCAAACC SEQ ID NO: 40FR-TCGATTATGAGGAGCTAAGAGAGCAAT SEQ ID NO: 41 ATTGCTCTCTTAGCTCCTCATAATCGASEQ ID NO: 42 GTAACGGCAGCATGTCCT SEQ ID NO: 43 TAGAGACTTTGTTGGTCAGCSEQ ID NO: 44 TGGTGAATGCCCCATAGCACGAG SEQ ID NO: 45AGAATGAACTATTACTGGACAC SEQ ID NO: 46 GGACTGGTGTATCTGAAATG SEQ ID NO: 47TAGAGCCGGGAGACAAAATAACATTC SEQ ID NO: 48 ACTGGAAATCTAGTGGTACCGAGATASEQ ID NO: 49 TACCAGATCCAGCATTTCTTTCCATTG SEQ ID NO: 50AGCACAAAATTGAGACTGGC SEQ ID NO: 51 CCTGCTCATTTTGATGGTG SEQ ID NO: 52CAGGATTGAGGAATGTCCCGTCTA SEQ ID NO: 53 ACCGTACCATCCATCTACCATCCSEQ ID NO: 54 ACAGTTCACAGCAGTAGGTA SEQ ID NO: 55 CTGGCTTCTTACCTTTTCATATSEQ ID NO: 56 TTGATGATGGTTTCCTGGACATTTGGA SEQ ID NO: 57TCTTCACATTTGAATCGTGGTAGTCCAAA SEQ ID NO: 58 TCATTTTCCAATAGAACCAACAGTTCGGSEQ ID NO: 59 GAAGCAAAATTAAACAGAGAAGAA SEQ ID NO: 60TAGAGCACATCCAGAAACTGA SEQ ID NO: 61 ATCAACAAGGATTTACCAGATTTTGGCGASEQ ID NO: 62 ACCAATGAACTGGCGACAGTTGAATAGA


27. The composition of claim 26, wherein the oligonucleotides are usedin combinations of oligonucleotides selected from the group consistingof: Combination 1: SEQ ID NO: 1 and SEQ ID NO:2; Combination 2: SEQ IDNO:5 and SEQ ID NO:6; Combination 3: SEQ ID NO:8 and SEQ ID NO:9;Combination 4: SEQ ID NO:12 and SEQ ID NO:13; Combination 5: SEQ IDNO:17 and SEQ ID NO:18; Combination 6: SEQ ID NO:21 and SEQ ID NO:22;Combination 7: SEQ ID NO:26 and SEQ ID NO:27; Combination 8: SEQ IDNO:30 and SEQ ID NO:31; Combination 9: SEQ ID NO:34 and SEQ ID NO:35;Combination 10: SEQ ID NO:38 and SEQ ID NO:39; Combination 11: SEQ IDNO:42 and SEQ ID NO:43; Combination 12: SEQ ID NO:45 and SEQ ID NO:46;Combination 13: SEQ ID NO:50 and SEQ ID NO:51; Combination 14: SEQ IDNO:54 and SEQ ID NO:55; and Combination 15: SEQ ID NO:59 and SEQ IDNO:60.
 28. The composition of claim 26, wherein the oligonucleotides areused in combinations selected from the group consisting of: Combination1: SEQ ID NO:1 and SEQ ID NO:2 with one or both of SEQ ID NO:3 and SEQID NO:4; Combination 2: SEQ ID Nos. 5, 6, and 7; Combination 3: SEQ IDNO:8 and SEQ ID NO:9 with one or both of SEQ ID NO:10 and SEQ ID NO:11;Combination 4: SEQ ID NO:12 and SEQ ID NO:13 with one or more of SEQ IDNos. 14, 15, and 16; Combination 5: SEQ ID NO:17 and SEQ ID NO:18 withone or both of SEQ ID NO:19 and SEQ ID NO:20; Combination 6: SEQ IDNO:21 and SEQ ID NO:22 with one or more of SEQ ID Nos. 23, 24, and 25;Combination 7: SEQ ID NO:26 and SEQ ID NO:27 with one or both of SEQ IDNO:28 and SEQ ID NO:29; Combination 8: SEQ ID NO:30 and SEQ ID NO:31with one or both of SEQ ID NO:32 and SEQ ID NO:33; Combination 9: SEQ IDNO:34 and SEQ ID NO:35 with one or both of SEQ ID NO:36 and SEQ IDNO:37; Combination 10: SEQ ID NO:38 and SEQ ID NO:39 with one or both ofSEQ ID NO:40 and SEQ ID NO:41; Combination 11: SEQ ID Nos. 42, 43, and44; Combination 12: SEQ ID NO:45 and SEQ ID NO:46 with one or more ofSEQ ID Nos. 47, 48 and 49; Combination 13: SEQ ID NO:50 and SEQ ID NO:51with one or both of SEQ ID NO:52 and SEQ ID NO:53; Combination 14: SEQID NO:54 and SEQ ID NO:55 with one or more of SEQ ID Nos. 56, 57, and58; and Combination 15: SEQ ID NO:59 and SEQ ID NO:60 with one or bothof SEQ ID NO:61 and SEQ ID NO:62.
 29. A composition for detecting thepresence of seasonal H1 influenza virus A comprising at least twooligonucleotides specific for sequences in that represent a H1 influenzavirus A genome or transcripts made from the H1 influenza virus A genome,selected from the group consisting of: SEQ ID NO: 63AGGTTTGTTTGGAGCCATTG SEQ ID NO: 64 TTGTTGAATTCTTTGCCCAC SEQ ID NO: 65TCATTGAAGGGGGGTGGACTGGAA SEQ ID NO: 66 TGGACTGGAATGGTAGATGGTTGGTSEQ ID NO: 67 TCATTTTCTCAATTACAGAATTCACCTTGTTTG SEQ ID NO: 68ATCATACAGAAAATGCTTATGT SEQ ID NO: 69 MAGCAGAGTCCAGTAGTA SEQ ID NO: 70TTCACATTATAGCAGAAGATTCACCCCAG SEQ ID NO: 71 ACCCCAGAAATAGCCAAAAGACCCSEQ ID NO: 72 TTGAGGCAAATGGAAATCTAATA SEQ ID NO: 73TACATTCTGGAAAGGAAGACT SEQ ID NO: 74 AGTAGAGGCTTTGGATCAGGAATCATCSEQ ID NO: 75 TGTTTATAGCTCCCTGAGGTGTTTGACA SEQ ID NO: 76CATTGGTGCATTTGAGGTGATGATTCCT


30. The composition of claim 29, wherein the oligonucleotides are usedin combinations selected from the group consisting of: Combination 1:SEQ ID NO:63 and SEQ ID NO:64; Combination 2: SEQ ID NO:68 and SEQ IDNO:69; and Combination 3: SEQ ID NO:72 and SEQ ID NO:73.
 31. Thecomposition of claim 29, wherein the oligonucleotides are used incombinations selected from the group consisting of: Combination 1: SEQID NO:63 and SEQ ID NO:64 with one or more of SEQ ID Nos. 65, 66, and67; Combination 2: SEQ ID NO:68 and SEQ ID NO:69 with one or both of SEQID NO:70 and SEQ ID NO:71; and Combination 3: SEQ ID NO:72 and SEQ IDNO:73 with one or more of SEQ ID Nos. 74, 75 and
 76. 32. A compositionfor detecting the presence of seasonal H3 influenza virus A comprisingat least two oligonucleotides specific for sequences in that represent aH3 influenza virus A genome or transcripts made from the H3 influenzavirus A genome, selected from the group consisting of: SEQ ID NO: 77ACTAATGCTACTGAGCTGGT SEQ ID NO: 78 CTTATTTTGGAAGCCATCACA SEQ ID NO: 79ATCCTTGATGGAGAAAACTGCACACTA SEQ ID NO: 80 AGGGTCTCCCAATAGAGCATCTATTAGSEQ ID NO: 81 TAGTGTGCAGTTTTCTCCATCAAGGAT SEQ ID NO: 82AAGACTATCATTGCTTTGAGCT SEQ ID NO: 83 TGAACCAGCTCAGTAGCATT SEQ ID NO: 84CTTCAATTTGGTCATTCGTGATTGTTTTCAC SEQ ID NO: 85 CTCTATTGGGAGACCCTCASEQ ID NO: 86 CTTTCATTGTTAAACTCCAGTG SEQ ID NO: 87TGTGATGGCTTCCAAAATAAGAAATGGGA SEQ ID NO: 88 TGCTCAAGCATCAGGAAGAATSEQ ID NO: 89 CCCTAGGAGCAATTAGATTC SEQ ID NO: 90TCTACCAAAAGAAGCCAACAAACTGTAAT SEQ ID NO: 91 TGCTGTTAATCAAAAGTATGTCTCCCGSEQ ID NO: 92 AGCTCAATAATGAGATCAGATG SEQ ID NO: 93 TTCCCTCCCAACCATTTTCTSEQ ID NO: 94 CCAAATGGAAGCATTCCCAATGACAAAC SEQ ID NO: 95CAAATATGCCTCTAGTTTGTTTCTCTGG SEQ ID NO: 96 TCTCAAAAGCACTCAAGCAGSEQ ID NO: 97 CTCCGCGTTGTATGACCA SEQ ID NO: 98CAAATCAATGGGAAGCTGAATAG(A/G)TTG SEQ ID NO: 99 CCTGGAGAACCAACATACAASEQ ID NO: 100 CAGGCATTGTCACATTTGTG SEQ ID NO: 101TGATCTAACTGACTCAGAAATGAACAAACT SEQ ID NO: 102 ATCCTCAGCATTTTCCCTCAGTTGCT


33. The composition of claim 32, wherein the oligonucleotides are usedin combinations selected from the group consisting of: Combination 1:SEQ ID NO:77 and SEQ ID NO:78; Combination 2: SEQ ID NO:82 and SEQ IDNO:83; Combination 3: SEQ ID NO:85 and SEQ ID NO:86; Combination 4: SEQID NO:88 and SEQ ID NO:89; Combination 5: SEQ ID NO:92 and SEQ ID NO:93;Combination 6: SEQ ID NO:96 and SEQ ID NO:97; and Combination 7: SEQ IDNO:99 and SEQ ID NO:100.
 34. The composition of claim 32, wherein theoligonucleotides are used in combinations selected from the groupconsisting of: Combination 1: SEQ ID NO:77 and SEQ ID NO:78 with one ormore of SEQ ID Nos. 79, 80 and 81; Combination 2: SEQ ID Nos. 82, 83 and84; Combination 3: SEQ ID Nos. 85, 86 and 87; Combination 4: SEQ IDNO:88 and SEQ ID NO:89 with one or both of SEQ ID NO:90 and SEQ IDNO:91; Combination 5: SEQ ID NO:92 and SEQ ID NO:93 with one or both ofSEQ ID NO:94 and SEQ ID NO:95; Combination 6: SEQ ID Nos. 96, 97 and 98;and Combination 7: SEQ ID NO:99 and SEQ ID NO:100 with one or both ofSEQ ID NO:101 and SEQ ID NO:102.
 35. A kit comprising, in a suitablecontainer, a composition according to any one of claims 26-34, andinstructions for use of said composition in any assay for amplificationof polynucleotides in a biological sample.
 36. A method for thedetection of an influenza A virus from a sample, comprising the stepsof: a. contacting an influenza A virus nucleic acid from a sample with acomposition according to any one of claim 1-8, 12-21 or 26-34; b.providing conditions for amplifying the nucleic acid from step a by apolymerase chain reaction to generate an amplification product from thenucleic acid; and c. detecting the presence or absence of amplificationproduct from step b, wherein the presence of the amplification productindicates that the sample contained an influenza A virus.
 37. The methodaccording to claim 36, wherein the detecting step is a real-timedetecting step.
 38. The method according to claim 37, wherein thedetecting step is a taqman PCR detecting step.
 39. The method accordingto claim 36, wherein the sample contains an influenza A virus nucleicacid selected from the group consisting of: a H1N1 influenza A virusnucleic acid, a seasonal H1 influenza A virus nucleic acid, a seasonalH3 influenza A virus, and a combination thereof, and an amplificationproduct is generated therefrom.
 40. The method according to claim 36,wherein the sample contains an influenza A virus nucleic acid that issubstantially identical to an influenza A virus selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid, a seasonal H1influenza A virus nucleic acid and a seasonal H3 influenza A virus, andan amplification product is generated therefrom.
 41. The methodaccording to claim 40, wherein the sample contains an influenza A virusnucleic acid that is at least 90% identical to an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid, a seasonal H1 influenza A virus nucleic acid and a seasonal H3influenza A virus, and an amplification product is generated therefrom.42. The method according to claim 36, wherein the sample contains aninfluenza A virus nucleic acid that has an H1 gene that is substantiallyidentical to the H1 gene of an influenza A virus selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid and a seasonal H1influenza A virus nucleic acid, and an amplification product isgenerated therefrom.
 43. The method according to claim 42, wherein thesample contains an influenza A virus nucleic acid that has an H1 genethat is at least 90% identical to the H1 gene of an influenza A virusselected from the group consisting of: a H1N1 influenza A virus nucleicacid and a seasonal H1 influenza A virus nucleic acid, and anamplification product is generated therefrom.
 44. The method accordingto claim 36, wherein the amplifying step is a multiplex amplificationreaction for detecting two or more of an influenza A virus nucleic acid,each of which are independently at least 90% identical to an influenza Avirus selected from the group consisting of: a H1N1 influenza A virusnucleic acid, a seasonal H1 influenza A virus nucleic acid and aseasonal H3 influenza A virus.
 45. A method for the detection of aninfluenza A virus from a sample, comprising the steps of: a. contactingan influenza A virus nucleic acid from a sample with a compositionaccording to one of Mixture 1 to Mixture 23; b. providing conditions foramplifying the nucleic acid from step a by a polymerase chain reactionto generate an amplification product from the nucleic acid; and c.detecting the presence or absence of amplification product from step b,wherein the presence of the amplification product indicates that thesample contained an influenza A virus.
 46. The method according to claim45, wherein the detecting step is a real-time detecting step.
 47. Themethod according to claim 46, wherein the detecting step is a taqman PCRdetecting step.
 48. The method according to claim 45, wherein the samplecontains an influenza A virus nucleic acid selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid, a seasonal H1influenza A virus nucleic acid, a seasonal H3 influenza A virus, and acombination thereof, and an amplification product is generatedtherefrom.
 49. The method according to claim 45, wherein the samplecontains an influenza A virus nucleic acid that is substantiallyidentical to an influenza A virus selected from the group consisting of:a H1N1 influenza A virus nucleic acid, a seasonal H1 influenza A virusnucleic acid and a seasonal H3 influenza A virus, and an amplificationproduct is generated therefrom.
 50. The method according to claim 49,wherein the sample contains an influenza A virus nucleic acid that is atleast 90% identical to an influenza A virus selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid, a seasonal H1influenza A virus nucleic acid and a seasonal H3 influenza A virus, andan amplification product is generated therefrom.
 51. The methodaccording to claim 45, wherein the sample contains an influenza A virusnucleic acid that has an H1 gene that is substantially identical to theH1 gene of an influenza A virus selected from the group consisting of: aH1N1 influenza A virus nucleic acid and a seasonal H1 influenza A virusnucleic acid, and an amplification product is generated therefrom. 52.The method according to claim 51, wherein the sample contains aninfluenza A virus nucleic acid that has an H1 gene that is at least 90%identical to the H1 gene of an influenza A virus selected from the groupconsisting of: a H1N1 influenza A virus nucleic acid and a seasonal H1influenza A virus nucleic acid, and an amplification product isgenerated therefrom.
 53. The method according to claim 45, wherein theamplifying step is a multiplex amplification reaction for detecting twoor more of an influenza A virus nucleic acid, each of which areindependently at least 90% identical to an influenza A virus selectedfrom the group consisting of: a H1N1 influenza A virus nucleic acid, aseasonal H1 influenza A virus nucleic acid and a seasonal H3 influenza Avirus.
 54. A method for the detection of an H1N1 Influenza A Virus froma sample, comprising the steps of: a. contacting an H1N1 Influenza AVirus from a sample with primer pair selected from Table 1; b. providingconditions for amplifying the nucleic acid from step a by a polymerasechain reaction to generate an amplification product from the nucleicacid; and c. detecting the presence or absence of amplification productfrom step b, wherein the presence of the amplification product indicatesthat the sample contained an H1N1 Influenza A Virus.
 55. The methodaccording to claim 54, wherein the detecting step is a real-timedetecting step.
 56. The method according to claim 55, wherein thedetecting step is a taqman PCR detecting step.
 57. The method accordingto any one of claims 54 to 56, wherein the detecting step uses a probeselected from Table
 1. 58. The method according to claim 54, wherein thesample further contains an influenza A virus nucleic acid selected fromthe group consisting of: a seasonal H1 influenza A virus nucleic acid, aseasonal H3 influenza A virus, and a combination thereof, and anamplification product is generated therefrom.
 59. The method accordingto claim 54, wherein the amplifying step is a multiplex amplificationreaction that further comprises a primer pair from Table 2, a primerpair from Table 3 or a primer pair from Table 2 and a primer pair fromTable
 3. 60. The method according to claim 59, wherein the detectingstep further comprises a probe from Table 2, a probe from Table 3 or aprobe from Table 2 and a probe from Table
 3. 61. The method according toclaim 59 or 60, wherein the amplifying step generates a detectableamplification product from an influenza A virus nucleic acid that is atleast 90% identical to an influenza A virus nucleic acid selected fromthe group consisting of: an H1N1 influenza virus nucleic acid, aseasonal H1 influenza A virus nucleic acid, a seasonal H3 influenza Avirus, and a combination thereof.
 62. The method according to claim 61,wherein the amplification product is detected using a taqman probehaving a nucleic acid sequence according to a probe sequence in Table 2or Table
 3. 63. A method for the detection of a seasonal H1 Influenza AVirus from a sample, comprising the steps of: a. contacting a seasonalH1 Influenza A Virus nucleic acid from a sample with primer pairselected from Table 2; b. providing conditions for amplifying thenucleic acid from step a by a polymerase chain reaction to generate anamplification product from the nucleic acid; and c. detecting thepresence or absence of amplification product from step b, wherein thepresence of the amplification product indicates that the samplecontained a seasonal H1 Influenza A Virus.
 64. The method according toclaim 63, wherein the detecting step is a real-time detecting step. 65.The method according to claim 64, wherein the detecting step is a taqmanPCR detecting step.
 66. The method according to any one of claims 63 to65, wherein the detecting step uses a probe selected from Table
 2. 67.The method according to claim 63, wherein the sample further contains aninfluenza A virus nucleic acid selected from the group consisting of: aH1N1 influenza A virus nucleic acid, a seasonal H3 influenza A virus,and a combination thereof, and an amplification product is generatedtherefrom.
 68. The method according to claim 63, wherein the amplifyingstep is a multiplex amplification reaction that further comprises aprimer pair from Table 1, a primer pair from Table 3 or a primer pairfrom Table 1 and a primer pair from Table
 3. 69. The method according toclaim 68, wherein the detecting step further comprises a probe fromTable 1, a probe from Table 3 or a probe from Table 1 and a probe fromTable
 3. 70. The method according to claim 68 or 69, wherein theamplifying step generates a detectable amplification product from aninfluenza A virus nucleic acid that is at least 90% identical to aninfluenza A virus nucleic acid selected from the group consisting of: aH1N1 influenza A virus nucleic acid, a seasonal H3 influenza A virus,and a combination thereof.
 71. A method for the detection of a seasonalH3 Influenza A Virus from a sample, comprising the steps of: a.contacting a seasonal H3 Influenza A Virus nucleic acid from a samplewith primer pair selected from Table 3; b. providing conditions foramplifying the nucleic acid from step a by a polymerase chain reactionto generate an amplification product from the nucleic acid; and c.detecting the presence or absence of amplification product from step b,wherein the presence of the amplification product indicates that thesample contained a seasonal H3 Influenza A Virus.
 72. The methodaccording to claim 71, wherein the detecting step is a real-timedetecting step.
 73. The method according to claim 72, wherein thedetecting step is a taqman PCR detecting step.
 74. The method accordingto any one of claims 71 to 73, wherein the detecting step uses a probeselected from Table
 3. 75. The method according to claim 71, wherein thesample further contains an influenza A virus nucleic acid selected fromthe group consisting of: a H1N1 influenza A virus nucleic acid, aseasonal H1 influenza A virus, and a combination thereof, and anamplification product is generated therefrom.
 76. The method accordingto claim 71, wherein the amplifying step is a multiplex amplificationreaction that further comprises a primer pair from Table 1, a primerpair from Table 2 or a primer pair from Table 1 and a primer pair fromTable
 2. 77. The method according to claim 76, wherein the detectingstep further comprises a probe from Table 1, a probe from Table 2 or aprobe from Table 1 and a probe from Table
 2. 78. The method according toclaim 76 or 77, wherein the amplifying step generates a detectableamplification product from an influenza A virus nucleic acid that is atleast 90% identical to an influenza A virus nucleic acid selected fromthe group consisting of: a H1N1 influenza A virus nucleic acid, aseasonal H1 influenza A virus, a seasonal H3 influenza A virus, and acombination thereof.
 79. The method according to any one of claims 24,25 and 36 to 78, further comprising a separating step wherein nucleicacids are removed from one or more other components in the sample. 80.The method according to claim 79, wherein the separating step takesplace before the amplifying step.
 81. The method according to claim 79or claim 80, wherein the separating step is performed using a targetcapture oligomer having a tail selected from the group consisting ofdT₀₋₃dA₁₂₋₃₀, and using a solid support having an immobilized probe thatis substantially complementary to the tail.
 82. The method according toclaim 79 or claim 80, wherein the separating step is a non-specificseparating step.